<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1 20151215//EN" "https://jats.nlm.nih.gov/publishing/1.1/JATS-journalpublishing1.dtd">
<article xmlns:xlink="http://www.w3.org/1999/xlink" specific-use="sps-1.9" dtd-version="1.1" xml:lang="pt" article-type="research-article">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">abc</journal-id>
      <journal-title-group>
        <journal-title>Arquivos Brasileiros de Cardiologia</journal-title>
        <abbrev-journal-title abbrev-type="publisher">Arq. Bras. Cardiol.</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0066-782X</issn>
      <issn pub-type="epub">1678-4170</issn>
      <publisher>
        <publisher-name>Sociedade Brasileira de Cardiologia - SBC</publisher-name>
        <publisher-loc>S&#227;o Paulo, SP, Brazil</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">k6hnrbQx3gRN964TvFPdyrv</article-id>
      <article-id pub-id-type="other">00005</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2010000400005</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(10)09400405</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2010005000016</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Preval&#234;ncia e impacto progn&#243;stico da disfun&#231;&#227;o diast&#243;lica na doen&#231;a renal cr&#244;nica em hemodi&#225;lise</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Barberato</surname>
            <given-names>Silvio H.</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Bucharles</surname>
            <given-names>S&#233;rgio G. E.</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Sousa</surname>
            <given-names>Admar M.</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Costantini</surname>
            <given-names>Costantino O.</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Costantini</surname>
            <given-names>Costantino R. F.</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Pecoits-Filho</surname>
            <given-names>Roberto</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="state">Paran&#225;</named-content>
        </addr-line>
        <institution content-type="orgname">Pontif&#237;cia Universidade Cat&#243;lica do Paran&#225;</institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="state">Paran&#225;</named-content>
        </addr-line>
        <institution content-type="orgname">Hospital Cardiol&#243;gico Costantini</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>04</month>
        <year>2010</year>
      </pub-date>
      <volume>94</volume>
      <issue>4</issue>
      <fpage>457</fpage>
      <lpage>462</lpage>
      <history>
        <date date-type="rev-recd">
          <day>18</day>
          <month>08</month>
          <year>2009</year>
        </date>
        <date date-type="received">
          <day>17</day>
          <month>02</month>
          <year>2009</year>
        </date>
        <date date-type="accepted">
          <day>27</day>
          <month>08</month>
          <year>2009</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/" xml:lang="en">
          <license-p>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>FUNDAMENTO: Disfun&#231;&#227;o diast&#243;lica &#233; frequente em pacientes de hemodi&#225;lise, mas seu impacto na evolu&#231;&#227;o cl&#237;nica &#233; incerto. OBJETIVO: Avaliar a preval&#234;ncia e o impacto progn&#243;stico da disfun&#231;&#227;o diast&#243;lica (DD) avan&#231;ada (DDA) do ventr&#237;culo esquerdo (VE) em pacientes de hemodi&#225;lise. M&#201;TODOS: Ecocardiogramas foram realizados em pacientes no primeiro ano de hemodi&#225;lise, em ritmo sinusal, sem doen&#231;a cardiovascular manifestada, excluindo-se aqueles com valvopatia significativa ou derrame peric&#225;rdico. Pela avalia&#231;&#227;o integrada dos dados ecodopplercardiogr&#225;ficos, a fun&#231;&#227;o diast&#243;lica foi classificada como: 1) normal, 2) DD discreta (altera&#231;&#227;o do relaxamento) e 3) DDA (pseudonormaliza&#231;&#227;o e fluxo restritivo). Os desfechos pesquisados foram mortalidade geral e eventos cardiovasculares. RESULTADOS: Foram inclu&#237;dos 129 pacientes (78 homens), com idade 52 &#177; 16 anos e preval&#234;ncia de DD de 73% (50% com DD discreta e 23% com DDA). No grupo com DDA, demonstrou-se maior idade (p &lt; 0,01), press&#227;o arterial sist&#243;lica (p &lt; 0,01) e diast&#243;lica (p = 0,043), massa do VE (p &lt; 0,01), &#237;ndice do volume do &#225;trio esquerdo (p &lt; 0,01) e propor&#231;&#227;o de diab&#233;ticos (p = 0,019), al&#233;m de menor fra&#231;&#227;o de eje&#231;&#227;o (p &lt; 0,01). Ap&#243;s 17 &#177; 7 meses, a mortalidade geral foi significativamente maior naqueles com DDA, em compara&#231;&#227;o aos normais e com DD discreta (p = 0,012, log rank test). Na an&#225;lise multivariada de Cox, a DDA foi preditiva de eventos cardiovasculares (hazard ratio 2,2, intervalo de confian&#231;a 1,1-4,3, p = 0,021) ap&#243;s ajuste para idade, g&#234;nero, diabete, massa do VE e fra&#231;&#227;o de eje&#231;&#227;o. CONCLUS&#195;O: A DDA subcl&#237;nica foi encontrada em aproximadamente um quarto dos pacientes de hemodi&#225;lise e acarretou impacto progn&#243;stico, independente de outros dados cl&#237;nicos e ecocardiogr&#225;ficos.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Doen&#231;as renais</kwd>
        <kwd>di&#225;lise renal</kwd>
        <kwd>disfun&#231;&#227;o do ventr&#237;culo esquerdo</kwd>
        <kwd>disfun&#231;&#227;o do ventr&#237;culo esquerdo</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>26</day>
        <month>03</month>
        <year>2010</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>ARTIGO ORIGINAL </p>
    <p> ECOCARDIOGRAFIA ADULTOS</p>
    <p>Preval&#234;ncia e impacto progn&#243;stico da disfun&#231;&#227;o diast&#243;lica na doen&#231;a renal cr&#244;nica em hemodi&#225;lise</p>
    <p>
      <bold>Silvio H. Barberato<sup>I,II</sup>; S&#233;rgio G. E. Bucharles<sup>I</sup>; Admar M. Sousa<sup>II</sup>; Costantino O. Costantini<sup>II</sup>; Costantino R. F. Costantini<sup>II</sup>; Roberto Pecoits-Filho<sup>I</sup></bold>
    </p>
    <p><sup>I</sup>Pontif&#237;cia Universidade Cat&#243;lica do Paran&#225; </p>
    <p><sup>II</sup>Hospital Cardiol&#243;gico Costantini, Curitiba, PR - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="nt">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO: </bold>Disfun&#231;&#227;o diast&#243;lica &#233; frequente em pacientes de hemodi&#225;lise, mas seu impacto na evolu&#231;&#227;o cl&#237;nica &#233; incerto. </p>
    <p><bold>OBJETIVO: </bold>Avaliar a preval&#234;ncia e o impacto progn&#243;stico da disfun&#231;&#227;o diast&#243;lica (DD) avan&#231;ada (DDA) do ventr&#237;culo esquerdo (VE) em pacientes de hemodi&#225;lise. </p>
    <p><bold>M&#201;TODOS: </bold>Ecocardiogramas foram realizados em pacientes no primeiro ano de hemodi&#225;lise, em ritmo sinusal, sem doen&#231;a cardiovascular manifestada, excluindo-se aqueles com valvopatia significativa ou derrame peric&#225;rdico. Pela avalia&#231;&#227;o integrada dos dados ecodopplercardiogr&#225;ficos, a fun&#231;&#227;o diast&#243;lica foi classificada como: 1) normal, 2) DD discreta (altera&#231;&#227;o do relaxamento) e 3) DDA (pseudonormaliza&#231;&#227;o e fluxo restritivo). Os desfechos pesquisados foram mortalidade geral e eventos cardiovasculares. </p>
    <p><bold>RESULTADOS: </bold>Foram inclu&#237;dos 129 pacientes (78 homens), com idade 52 &#177; 16 anos e preval&#234;ncia de DD de 73% (50% com DD discreta e 23% com DDA). No grupo com DDA, demonstrou-se maior idade (p &lt; 0,01), press&#227;o arterial sist&#243;lica (p &lt; 0,01) e diast&#243;lica (p = 0,043), massa do VE (p &lt; 0,01), &#237;ndice do volume do &#225;trio esquerdo (p &lt; 0,01) e propor&#231;&#227;o de diab&#233;ticos (p = 0,019), al&#233;m de menor fra&#231;&#227;o de eje&#231;&#227;o (p &lt; 0,01). Ap&#243;s 17 &#177; 7 meses, a mortalidade geral foi significativamente maior naqueles com DDA, em compara&#231;&#227;o aos normais e com DD discreta (p = 0,012, <italic>log rank test</italic>). Na an&#225;lise multivariada de Cox, a DDA foi preditiva de eventos cardiovasculares (<italic>hazard ratio</italic> 2,2, intervalo de confian&#231;a 1,1-4,3, p = 0,021) ap&#243;s ajuste para idade, g&#234;nero, diabete, massa do VE e fra&#231;&#227;o de eje&#231;&#227;o. </p>
    <p><bold>CONCLUS&#195;O:</bold> A DDA subcl&#237;nica foi encontrada em aproximadamente um quarto dos pacientes de hemodi&#225;lise e acarretou impacto progn&#243;stico, independente de outros dados cl&#237;nicos e ecocardiogr&#225;ficos. </p>
    <p><bold>Palavras-chave:</bold> Doen&#231;as renais, di&#225;lise renal, disfun&#231;&#227;o do ventr&#237;culo esquerdo/fisiopatologia/terapia.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>As complica&#231;&#245;es cardiovasculares s&#227;o as principais causas de &#243;bito nos pacientes portadores de doen&#231;a renal cr&#244;nica (DRC) em terapia de substitui&#231;&#227;o renal pela hemodi&#225;lise (HD)<sup>1</sup>. Nesses indiv&#237;duos, o achado de altera&#231;&#245;es ecocardiogr&#225;ficas do ventr&#237;culo esquerdo (VE), como hipertrofia, dilata&#231;&#227;o e disfun&#231;&#227;o sist&#243;lica, triplica o risco de insufici&#234;ncia card&#237;aca, independente de idade, presen&#231;a de diabete e insufici&#234;ncia coronariana<sup>2</sup>. Por outro lado, embora as altera&#231;&#245;es do enchimento ventricular esquerdo sejam frequentemente detectadas nesse grupo, a preval&#234;ncia real da disfun&#231;&#227;o diast&#243;lica (DD) e seu impacto na evolu&#231;&#227;o cl&#237;nica n&#227;o s&#227;o conhecidos<sup>3,4</sup>. Do ponto de vista hemodin&#226;mico, a eleva&#231;&#227;o da press&#227;o diast&#243;lica intraventricular esquerda &#233; o fen&#244;meno respons&#225;vel pela manifesta&#231;&#227;o da insufici&#234;ncia card&#237;aca, qualquer que seja a causa subjacente<sup>5</sup>. Portanto, torna-se oportuno detectar a presen&#231;a da DD avan&#231;ada (DDA), caracterizada pelo aumento das press&#245;es de enchimento, sobretudo na fase subcl&#237;nica. Nesse contexto, t&#233;cnicas ecodopplercardiogr&#225;ficas relativamente independentes da pr&#233;-carga, como o Doppler tecidual<sup>6</sup> e o volume do &#225;trio esquerdo<sup>7</sup>, representam importante avan&#231;o na avalia&#231;&#227;o da fun&#231;&#227;o diast&#243;lica. Os objetivos deste estudo s&#227;o estimar a preval&#234;ncia, identificar fatores predisponentes e avaliar o impacto progn&#243;stico da DDA do VE em indiv&#237;duos iniciando HD sem doen&#231;a cardiovascular clinicamente manifesta.</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>
      <bold>Popula&#231;&#227;o</bold>
    </p>
    <p>Foram considerados eleg&#237;veis para o estudo pacientes portadores de DRC que estavam em programa de HD de manuten&#231;&#227;o (sess&#245;es com dura&#231;&#227;o de 4 horas, tr&#234;s vezes por semana) em dois servi&#231;os de nefrologia baseados em hospitais universit&#225;rios. Os crit&#233;rios de inclus&#227;o foram: estar sob terapia hemodial&#237;tica entre um e 12 meses, aus&#234;ncia de afec&#231;&#245;es cardiovasculares pregressas (insufici&#234;ncia card&#237;aca congestiva, infarto agudo do mioc&#225;rdio, acidente vascular cerebral ou insufici&#234;ncia arterial perif&#233;rica) e assinatura do termo de consentimento. Os crit&#233;rios de exclus&#227;o foram: malignidades, infec&#231;&#227;o ativa, ritmo card&#237;aco n&#227;o sinusal, valvopatia significativa (pr&#243;tese valvar, qualquer grau de estenose mitral ou a&#243;rtica, e insufici&#234;ncia mitral, a&#243;rtica ou tric&#250;spide moderada a importante), derrame peric&#225;rdico e ecocardiograma tecnicamente insatisfat&#243;rio. Todos os pacientes foram submetidos &#224; di&#225;lise com m&#225;quinas Altra Touch (Althin, Miami, Florida, Fl, USA) contendo dialisador de acetato celulose regulado com fluxo de sangue m&#237;nimo de 200 ml/minuto e fluxo do dialisato de 300 a 500 ml/minuto. A estimativa do "peso seco" (volume a ser retirado por ultrafiltra&#231;&#227;o) foi realizada por meio de sinais cl&#237;nicos de hidrata&#231;&#227;o, comportamento da press&#227;o arterial durante a sess&#227;o e bioimped&#226;ncia el&#233;trica<sup>8</sup>. A superf&#237;cie corp&#243;rea foi calculada de acordo com a equa&#231;&#227;o de Du Bois e Du Bois (0,20247 x peso<sup>0,425 </sup>x altura<sup>0,725</sup>). O &#237;ndice de massa corp&#243;rea foi calculado pela divis&#227;o do peso (kg) pelo quadrado da altura (m), considerando-se obesidade quando &gt; 30. Medimos press&#227;o arterial sist&#243;lica e diast&#243;lica, frequ&#234;ncia card&#237;aca, peso e altura no momento do exame. O comit&#234; de &#233;tica em pesquisa de nossa institui&#231;&#227;o aprovou o protocolo do estudo e o consentimento informado foi obtido de todos os pacientes.</p>
    <p>
      <bold>Ecodopplercardiograma</bold>
    </p>
    <p>Os exames foram realizados em dia interdial&#237;tico, com hor&#225;rio marcado entre 12 e 18 horas. Os pacientes foram posicionados em dec&#250;bito lateral esquerdo, utilizando-se ecocardi&#243;grafo Envisor C (Phillips Inc., Andover, Massachusetts, EUA) equipado com transdutores de 2 a 4 MHz para a realiza&#231;&#227;o de estudo completo pelos modos M, bidimensional e Doppler (puls&#225;til, cont&#237;nuo, colorido e tecidual). Os seguintes par&#226;metros foram obtidos ao modo M: di&#226;metro anteroposterior do &#225;trio esquerdo, espessura do septo interventricular e da parede posterior na di&#225;stole, di&#226;metro diast&#243;lico final (dilata&#231;&#227;o quando &gt; 54 mm para mulheres e &gt; 56 mm para homens) e sist&#243;lico final do VE. A massa ventricular esquerda foi estimada pela equa&#231;&#227;o de Devereux<sup>9</sup> e indexada pela altura elevada &#224; 2,7<sup>10</sup>. Definiu-se como hipertrofia ventricular esquerda a presen&#231;a de massa/altura<sup>2,7</sup><underline>&gt;</underline> 45 g/m<sup>2,7</sup> para mulheres e <underline>&gt;</underline> 49 g/m<sup>2,7 </sup>para homens<sup>11</sup>. A fun&#231;&#227;o sist&#243;lica foi avaliada pelo c&#225;lculo da fra&#231;&#227;o de eje&#231;&#227;o pelo m&#233;todo de Simpson<sup>11</sup>. As velocidades do fluxo transvalvar mitral foram registradas no corte apical 4 c&#226;maras com a amostra do Doppler puls&#225;til posicionada entre as extremidades das c&#250;spides da valva mitral, medindo-se as velocidades de enchimento r&#225;pido precoce (onda E), de contra&#231;&#227;o atrial (onda A) e rela&#231;&#227;o E/A. As velocidades do Doppler tecidual foram registradas no corte apical 4 c&#226;maras com uma amostra de volume posicionada consecutivamente na jun&#231;&#227;o das paredes lateral e septal do VE com o anel mitral<sup>12</sup>. Foram analisadas a velocidade diast&#243;lica precoce (E') e tardia (A') do anel, e calculadas as rela&#231;&#245;es E'/A' e E/E' (m&#233;dia dos lados do anel). O volume do &#225;trio esquerdo foi determinado ao bidimensional pela t&#233;cnica biplanar de Simpson<sup>11</sup> e indexado para a superf&#237;cie corp&#243;rea. Em todas as medidas considerou-se m&#233;dia de tr&#234;s ciclos card&#237;acos. </p>
    <p>
      <bold>Avalia&#231;&#227;o da fun&#231;&#227;o diast&#243;lica</bold>
    </p>
    <p>A fun&#231;&#227;o diast&#243;lica do VE foi categorizada a partir da interpreta&#231;&#227;o conjunta dos &#237;ndices derivados do Doppler convencional e Doppler tecidual do anel mitral em 4 padr&#245;es: normal, altera&#231;&#227;o do relaxamento (rela&#231;&#227;o E/A &lt; 1 e E' &lt; 10 cm/s), pseudonormal e fluxo restritivo (rela&#231;&#227;o E/A &gt; 2 e E'&lt; 8 cm/s)<sup>13</sup>. Para diagn&#243;stico do padr&#227;o pseudonormal (diferenciando do normal verdadeiro), foram utilizados os seguintes crit&#233;rios: a) rela&#231;&#227;o E/E' &gt; 15<sup>13</sup>; ou b) rela&#231;&#227;o E/E' <underline>&gt;</underline> 11<sup>12</sup>, associada ao &#237;ndice do volume do &#225;trio esquerdo &gt; 35 ml/m<sup>2,14</sup>. A amostra foi classificada posteriormente em tr&#234;s grupos, de acordo com o padr&#227;o hemodin&#226;mico de enchimento ventricular: 1) fun&#231;&#227;o diast&#243;lica normal, 2) DD discreta (DDD) (altera&#231;&#227;o do relaxamento) e 3) DDA (englobando fluxo restritivo e pseudonormaliza&#231;&#227;o). </p>
    <p>
      <bold>An&#225;lise de sobrevida</bold>
    </p>
    <p>Dados demogr&#225;ficos, comorbidades (diabete melito, hipertens&#227;o arterial, dislipidemia, tabagismo), drogas em uso e achados laboratoriais rotineiros foram levantados a partir de rigorosa an&#225;lise de prontu&#225;rio, al&#233;m de entrevista com o m&#233;dico respons&#225;vel, quando necess&#225;rio. Os desfechos prim&#225;rio e secund&#225;rio foram, respectivamente, mortalidade geral e um combinado de eventos cardiovasculares fatais e n&#227;o fatais. Os eventos pesquisados foram morte cardiovascular (incluindo morte s&#250;bita, infarto agudo do mioc&#225;rdio, acidente vascular cerebral), infarto do mioc&#225;rdio n&#227;o fatal e insufici&#234;ncia card&#237;aca congestiva descompensada (requerendo interna&#231;&#227;o hospitalar). O seguimento foi baseado na an&#225;lise dos desfechos realizada de forma peri&#243;dica, diretamente na cl&#237;nica de di&#225;lise. Pacientes que realizaram transplante renal ou mudaram de modalidade de di&#225;lise foram censurados.</p>
    <p>
      <bold>An&#225;lise estat&#237;stica</bold>
    </p>
    <p>An&#225;lise descritiva adequada foi aplicada para vari&#225;veis cont&#237;nuas (m&#233;dia e desvio-padr&#227;o) e categ&#243;ricas (porcentual). Compara&#231;&#245;es entre os grupos foram feitas por an&#225;lise de vari&#226;ncia (ANOVA, com corre&#231;&#227;o <italic>post hoc</italic> de Dunnett) para vari&#225;veis cont&#237;nuas, e por testes de qui-quadrado para vari&#225;veis categ&#243;ricas. An&#225;lise de regress&#227;o log&#237;stica determinou os preditores independentes da DD. Curvas de sobrevida de Kaplan-Meier para o estado da fun&#231;&#227;o diast&#243;lica foram constru&#237;das e comparadas pelo teste <italic>log rank</italic>. O impacto progn&#243;stico independente da DD foi avaliado pela an&#225;lise multivariada de sobrevida de Cox, levando-se em conta preditores estabelecidos de risco nesta popula&#231;&#227;o. N&#237;vel de signific&#226;ncia estat&#237;stica foi definido como p &lt; 0,05. Os programas estat&#237;sticos <italic>SPSS 13 for Windows</italic> e <italic>JMP IN 5.1</italic> foram utilizados.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>
      <bold>Caracter&#237;sticas basais</bold>
    </p>
    <p>As caracter&#237;sticas demogr&#225;ficas, cl&#237;nicas, bioqu&#237;micas e ecodopplercardiogr&#225;ficas dos 129 pacientes que formaram a popula&#231;&#227;o do estudo est&#227;o expostas na <xref ref-type="table" rid="tab01">Tabela 1</xref>. Nosso grupo constitui-se de 78 homens e 51 mulheres, com idade m&#233;dia de 52 &#177; 16 anos e dura&#231;&#227;o da di&#225;lise de 7 &#177; 4 meses. A etiologia da DRC foi atribu&#237;da &#224; nefroesclerose hipertensiva (39%), nefropatia diab&#233;tica (21%), associa&#231;&#227;o das duas anteriores (15%), glomerulonefrite cr&#244;nica (14%), rim polic&#237;stico (5%), lit&#237;ase (3%), pielonefrite cr&#244;nica (2%) e outras afec&#231;&#245;es (1%). A maioria dos pacientes (77%) estava em uso de medica&#231;&#227;o anti-hipertensiva, em especial os inibidores da enzima conversora (46%), betabloqueadores (16%), alfabloqueadores (13%), antagonistas dos canais de c&#225;lcio (12%) e bloqueadores dos receptores da angiotensina (11%), isolados ou em associa&#231;&#227;o.</p>
    <table-wrap id="tab01">
      <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt01.jpg"/></table-wrap>
    <p>
      <bold>Altera&#231;&#245;es cl&#237;nicas e ecodopplercardiogr&#225;ficas </bold>
    </p>
    <p>Ao ingressar no estudo, 45% tinham hipertens&#227;o arterial, 34% diabete melito, 25% dislipidemia e 11% eram tabagistas. A preval&#234;ncia de obesidade (IMC &gt; 30) foi 9%. A dilata&#231;&#227;o do VE estava presente em 34 pacientes (26%), hipertrofia em 110 (85%) e disfun&#231;&#227;o sist&#243;lica em 24 (19%), isoladas ou em associa&#231;&#227;o. Somente 19 (15%) tinham geometria normal do VE. Dilata&#231;&#227;o significativa do &#225;trio esquerdo (volume &gt; 32ml/m<sup>2</sup>) foi encontrada em 58 indiv&#237;duos (45%).</p>
    <p>
      <bold>Preval&#234;ncia da disfun&#231;&#227;o diast&#243;lica</bold>
    </p>
    <p>DD foi diagnosticada em 94 dos 129 pacientes (73%), sendo 64 com DD discreta (50%) e 30 com DD avan&#231;ada (23%). Neste &#250;ltimo grupo, havia 20 pacientes com pseudonormaliza&#231;&#227;o e 10 com fluxo restritivo. Em paralelo, apenas 22 (17%) tinham rela&#231;&#227;o E/E' m&#233;dia acima de 15. Ao se examinar exclusivamente as informa&#231;&#245;es do Doppler convencional, s&#243; 80 dos 129 pacientes estudados (62%) teriam a DD detectada.</p>
    <p>
      <bold>Preditores da DD avan&#231;ada</bold>
    </p>
    <p>As principais diferen&#231;as entre os grupos com fun&#231;&#227;o diast&#243;lica normal, DD discreta e DD avan&#231;ada est&#227;o listadas na <xref ref-type="table" rid="tab02">Tabela 2</xref>. Os indiv&#237;duos com DD avan&#231;ada tinham maior idade (p &lt; 0,01), press&#227;o arterial sist&#243;lica (p &lt; 0,01), press&#227;o arterial diast&#243;lica (0,043), massa do VE (p &lt; 0,01) e &#237;ndice do volume do &#225;trio esquerdo (p &lt; 0,01), bem como maior propor&#231;&#227;o de diab&#233;ticos (p = 0,019) e menor m&#233;dia de fra&#231;&#227;o de eje&#231;&#227;o (p &lt; 0,01). Ap&#243;s an&#225;lise de regress&#227;o log&#237;stica multivariada usando o grupo fun&#231;&#227;o normal como controle, os preditores independentes da DD avan&#231;ada foram diabetes (odds ratio [OR] 2, IC 1,6-5,9, p = 0,011), press&#227;o arterial sist&#243;lica (OR 1,05, IC 1,01-1,09, p = 0,023) e massa do VE (OR 1,06, intervalo de confian&#231;a [IC] 1,01-1,1, p &lt; 0,01), al&#233;m de tend&#234;ncia para a fra&#231;&#227;o de eje&#231;&#227;o (p = 0,052).</p>
    <table-wrap id="tab02">
      <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt02.jpg"/></table-wrap>
    <p>
      <bold>Desfechos</bold>
    </p>
    <p>Durante o seguimento m&#233;dio de 17 &#177; 7 meses, houve 26 &#243;bitos (20%) e 21 eventos cardiovasculares n&#227;o fatais (16%). As mortes foram atribu&#237;das a causas cardiovasculares (18 &#243;bitos, sendo 8 por infarto do mioc&#225;rdio, 7 por morte s&#250;bita, dois por arritmia ventricular complexa documentada e um por acidente vascular cerebral hemorr&#225;gico) e infecciosas (8 &#243;bitos). Os eventos cardiovasculares n&#227;o fatais foram infarto mioc&#225;rdico (5) e interna&#231;&#245;es por insufici&#234;ncia card&#237;aca descompensada (16), contabilizando 39 eventos cardiovasculares combinados no total. Como mostrado na <xref ref-type="fig" rid="fig01">Figura 1</xref> e na <xref ref-type="table" rid="tab03">Tabela 3</xref>, a mortalidade geral foi maior no grupo com DD avan&#231;ada (37%), em compara&#231;&#227;o aos normais e com DD discreta (9% e 19%, respectivamente, <italic>log rank test</italic>, p = 0,012). V&#225;rias an&#225;lises foram realizadas utilizando-se modelos multivariados de Cox. Ap&#243;s avalia&#231;&#227;o de mortalidade geral e eventos cardiovasculares em separado (modelos incluindo idade, sexo masculino, diabete, massa do VE e fra&#231;&#227;o de eje&#231;&#227;o), massa e fra&#231;&#227;o de eje&#231;&#227;o emergiram como preditores independentes para ambos os desfechos, al&#233;m de idade apenas para eventos cardiovasculares. A inclus&#227;o da DD avan&#231;ada nesses modelos alcan&#231;ou valor estat&#237;stico significativo para a predi&#231;&#227;o de eventos cardiovasculares (<italic>hazard ratio</italic> [HR] 2,2, IC 1,1-4,3, p = 0,021) e lim&#237;trofe para a mortalidade geral (HR 2,8, IC 0,97-8,2, p = 0,056), como visto na <xref ref-type="table" rid="tab04">Tabela 4</xref>. Em contraste, n&#227;o houve diferen&#231;as nos desfechos entre pacientes com e sem rela&#231;&#227;o E/E' &gt; 15 ou E'&lt; 8 cm/s. Em an&#225;lise alternativa, DD avan&#231;ada e &#237;ndice do volume de &#225;trio esquerdo (recentemente descrito como preditor do progn&#243;stico em pacientes de HD<sup>15</sup>) foram inclu&#237;dos em conjunto no &#250;ltimo passo do modelo. Foram preditivos de eventos cardiovasculares tanto DD avan&#231;ada (HR 3,4, IC 1,3-9,2, p = 0,03) como &#237;ndice do volume de &#225;trio esquerdo (HR 6,6, IC 1,8-24, p = 0,004).</p>
    <fig id="fig01">
      <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gf01.jpg"/></fig>
    <table-wrap id="tab03">
      <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt03.jpg"/></table-wrap>
    <table-wrap id="tab04">
      <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt04.jpg"/></table-wrap>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>Nosso estudo sugere que quase tr&#234;s quartos dos indiv&#237;duos no primeiro ano de HD tenham DD, sendo que em aproximadamente um quarto deles existe DDA. Estudos com casu&#237;sticas reduzidas reportaram preval&#234;ncia de DD em 50%-65% dos pacientes ur&#234;micos, incluindo popula&#231;&#245;es pr&#233;-di&#225;lise, em di&#225;lise e p&#243;s-transplante<sup>4</sup> (porcentual similar ao encontrado em nosso grupo, caso fossem desconsideradas as informa&#231;&#245;es do Doppler tecidual e volume do &#225;trio esquerdo). Tais an&#225;lises foram limitadas pela utiliza&#231;&#227;o de par&#226;metros derivados do fluxo transvalvar mitral e do fluxo venoso pulmonar para a categoriza&#231;&#227;o da fun&#231;&#227;o diast&#243;lica<sup>16</sup>. Sabe-se que esses m&#233;todos s&#227;o particularmente vulner&#225;veis &#224;s varia&#231;&#245;es da pr&#233;-carga<sup>6</sup>; portanto, tal abordagem pode ter induzido resultados falso-negativos, diagnosticando como normais portadores de pseudonormaliza&#231;&#227;o (altas press&#245;es de enchimento mascarando a altera&#231;&#227;o de relaxamento do VE). Nesse contexto, integrar as informa&#231;&#245;es do Doppler convencional com t&#233;cnicas relativamente independentes da pr&#233;-carga, como o Doppler tecidual e o volume do &#225;trio esquerdo, acrescenta precis&#227;o ao diagn&#243;stico da DD, em especial da DDA, caracterizada por alta press&#227;o intraventricular diast&#243;lica. Detectar a presen&#231;a da DD e estimar as press&#245;es de enchimento do VE &#233; de interesse geral nos dias atuais para a predi&#231;&#227;o do risco de desenvolver a chamada "insufici&#234;ncia card&#237;aca com fra&#231;&#227;o de eje&#231;&#227;o preservada". A insufici&#234;ncia card&#237;aca clinicamente manifesta representa um preditor independente de mortalidade nos pacientes iniciando terapia hemodial&#237;tica<sup>17</sup>, mas o discernimento da causa subjacente pode ser importante para direcionar a conduta terap&#234;utica. Estudos de necropsia e uremia experimental apontaram a presen&#231;a de fibrose intermiocardioc&#237;tica difusa espec&#237;fica no cora&#231;&#227;o de indiv&#237;duos ur&#234;micos, que poderia predispor &#224; instabilidade el&#233;trica (associada com morte s&#250;bita) e eleva&#231;&#227;o das press&#245;es de enchimento<sup>18,19</sup>. A interven&#231;&#227;o sobre os mecanismos fisiopatol&#243;gicos relacionados &#224; fibrose mioc&#225;rdica proeminente, como a ativa&#231;&#227;o de fatores humorais (angiotensina II, horm&#244;nio paratireoidiano, endotelina, aldosterona e catecolaminas plasm&#225;ticas)<sup>3</sup>, poder&#225; representar importante alvo terap&#234;utico, em especial na fase subcl&#237;nica.</p>
    <p>Apesar de tais considera&#231;&#245;es, pouco se investigou se o diagn&#243;stico da DDA colabora para refinar a estratifica&#231;&#227;o do risco cardiovascular no paciente ur&#234;mico. Recentemente, dois estudos tentaram estimar o impacto progn&#243;stico da DDA na DRC utilizando a rela&#231;&#227;o E/E', reconhecido &#237;ndice n&#227;o invasivo das press&#245;es de enchimento do VE na popula&#231;&#227;o geral<sup>12,20</sup>. Em estudo com 125 candidatos ao transplante renal, Sharma e cols.<sup>21</sup> encontraram associa&#231;&#227;o de E/E' &gt; 15 com maior mortalidade geral. Entretanto, a popula&#231;&#227;o do estudo foi heterog&#234;nea (apenas um ter&#231;o dos pacientes estava sob HD) e somente an&#225;lise univariada foi realizada, n&#227;o tornando poss&#237;vel inferir se E/E' acrescenta valor progn&#243;stico &#224; avalia&#231;&#227;o tradicional de risco cardiovascular neste grupo. J&#225; Wang e cols.<sup>22</sup> relataram, em pesquisa com 220 pacientes (exclusivamente de di&#225;lise peritoneal), que E/E' &gt; 15 foi capaz de prever mortalidade geral e card&#237;aca acima dos dados cl&#237;nicos e ecocardiogr&#225;ficos cl&#225;ssicos. Em nossa popula&#231;&#227;o, composta somente por pacientes de HD, a rela&#231;&#227;o E/E' &gt; 15 n&#227;o teve poder discriminador em rela&#231;&#227;o aos desfechos estudados. A fisiopatologia da doen&#231;a cardiovascular em indiv&#237;duos sob HD &#233; influenciada pelas abruptas e extensas varia&#231;&#245;es da volemia &#224;s quais esses pacientes s&#227;o submetidos<sup>23</sup>. A predi&#231;&#227;o acurada das press&#245;es de enchimento (e, por conseguinte, do progn&#243;stico) para um dado indiv&#237;duo requer a incorpora&#231;&#227;o de todos os dados dispon&#237;veis, o que torna a abordagem integrada mais consistente que um par&#226;metro tomado isoladamente. </p>
    <p>Entre as limita&#231;&#245;es do estudo &#233; importante mencionar o tamanho relativamente limitado da amostra, que foi contrabalanceado, no entanto, pelo adequado poder estat&#237;stico alcan&#231;ado (86% para desfecho prim&#225;rio e 94% para secund&#225;rio). Outras limita&#231;&#245;es foram a aus&#234;ncia de medidas invasivas das press&#245;es de enchimento do VE (quest&#245;es pr&#225;ticas e &#233;ticas n&#227;o justificariam cateterismo card&#237;aco na popula&#231;&#227;o estudada) e o rigor dos crit&#233;rios de exclus&#227;o (que podem ter tornado nossos achados n&#227;o aplic&#225;veis &#224; totalidade da popula&#231;&#227;o em di&#225;lise).</p>
    <p>
      <bold>Conclus&#245;es</bold>
    </p>
    <p>O presente estudo indica que a DDA, diagnosticada a partir da interpreta&#231;&#227;o combinada das informa&#231;&#245;es ecodopplercardiogr&#225;ficas, acarreta impacto progn&#243;stico em pacientes de HD sem eventos cardiovasculares pr&#233;vios. A mortalidade geral foi significativamente maior no grupo com DDA, em compara&#231;&#227;o aos normais e com DD discreta. Em paralelo, a DDA foi preditiva de eventos cardiovasculares independente de idade, g&#234;nero, diabete, massa do VE e fra&#231;&#227;o de eje&#231;&#227;o. </p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
    <p>
      <bold>Fontes de Financiamento</bold>
    </p>
    <p>O presente estudo foi parcialmente financiado por Bolsa de apoio para pesquisa em cardiologia da SBC.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>N&#227;o h&#225; vincula&#231;&#227;o deste estudo a programas de p&#243;s-gradua&#231;&#227;o.</p>
    <p>
      <fn id="nt" fn-type="corresp">
        <label>
          <bold> Correspond&#234;ncia:</bold>
        </label>
        <p> Silvio Henrique Barberato </p>
        <p> Rua Saint Hilaire, 122/203 - &#193;gua Verde </p>
        <p> 80240-140 - Curitiba, PR - Brasil </p>
        <p> E-mail: </p>
        <p><email xlink:href="silviohb@cardiol.br">silviohb@cardiol.br</email>, </p>
        <p>
          <email xlink:href="msbarberato@terra.com.br">msbarberato@terra.com.br</email>
        </p>
      </fn>
    </p>
    <p> Artigo recebido em 17/02/09; revisado recebido em 18/08/09; aceito em 27/08/09.</p>
  </body>
  <back>
    <ref-list>
      <ref id="B1">
        <mixed-citation>1. Sarnak MJ, Levey AS, Schoolwerth AC, Coresh    J, Culleton B, Hamm LL, et al. Kidney disease as a risk factor for development    of cardiovascular disease: a statement from the American Heart Association Councils    on Kidney in Cardiovascular Disease, High Blood Pressure Research, Clinical    Cardiology, and Epidemiology and Prevention. Circulation. 2003; 108: 2154-69.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Kidney disease as a risk factor for development of cardiovascular disease: a statement from the American Heart Association Councils on Kidney in Cardiovascular Disease, High Blood Pressure Research, Clinical Cardiology, and Epidemiology and Prevention</article-title>
          <source>Circulation</source>
          <date>
            <year>2003</year>
          </date>
          <fpage>2154</fpage>
          <lpage>69</lpage>
          <volume>108</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Sarnak</surname>
              <given-names>MJ</given-names>
            </name>
            <name>
              <surname>Levey</surname>
              <given-names>AS</given-names>
            </name>
            <name>
              <surname>Schoolwerth</surname>
              <given-names>AC</given-names>
            </name>
            <name>
              <surname>Coresh</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Culleton</surname>
              <given-names>B</given-names>
            </name>
            <name>
              <surname>Hamm</surname>
              <given-names>LL</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B2">
        <mixed-citation>2. Parfrey PS, Foley RN, Harnett JD, Kent    GM, Murray D, Barre PE. Outcome and risk factors of ischemic heart disease in    chronic uremia. Kidney Int. 1996; 49: 1428-34.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Outcome and risk factors of ischemic heart disease in chronic uremia</article-title>
          <source>Kidney Int</source>
          <date>
            <year>1996</year>
          </date>
          <fpage>1428</fpage>
          <lpage>34</lpage>
          <volume>49</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Parfrey</surname>
              <given-names>PS</given-names>
            </name>
            <name>
              <surname>Foley</surname>
              <given-names>RN</given-names>
            </name>
            <name>
              <surname>Harnett</surname>
              <given-names>JD</given-names>
            </name>
            <name>
              <surname>Kent</surname>
              <given-names>GM</given-names>
            </name>
            <name>
              <surname>Murray</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Barre</surname>
              <given-names>PE</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B3">
        <mixed-citation>3. London GM. Left ventricular alterations    and end-stage renal disease. Nephrol Dial Transplant. 2002; 17 (Suppl 1): 29-36.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Left ventricular alterations and end-stage renal disease</article-title>
          <source>Nephrol Dial Transplant</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>29</fpage>
          <lpage>36</lpage>
          <volume>17</volume>
          <person-group person-group-type="author">
            <name>
              <surname>London</surname>
              <given-names>GM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B4">
        <mixed-citation>4. Barberato SH, Pecoits Filho R. Altera&#231;&#245;es    ecocardiogr&#225;ficas em pacientes de hemodi&#225;lise. Arq Bras Cardiol.    2009. [In press]</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Altera&#231;&#245;es ecocardiogr&#225;ficas em pacientes de hemodi&#225;lise</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2009</year>
          </date>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Pecoits Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B5">
        <mixed-citation>5. Oh JK. Echocardiography as a noninvasive    Swan-Ganz catheter. Circulation. 2005; 111: 3192-4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Echocardiography as a noninvasive Swan-Ganz catheter</article-title>
          <source>Circulation</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>3192</fpage>
          <lpage>4</lpage>
          <volume>111</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Oh</surname>
              <given-names>JK</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B6">
        <mixed-citation>6. Barberato SH, Pecoits Filho R. Influence    of preload reduction on Tei index and other Doppler echocardiographic parameters    of left ventricular function. Arq Bras Cardiol. 2006; 86: 425-31.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Influence of preload reduction on Tei index and other Doppler echocardiographic parameters of left ventricular function</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2006</year>
          </date>
          <fpage>425</fpage>
          <lpage>31</lpage>
          <volume>86</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Pecoits Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B7">
        <mixed-citation>7. Barberato SH, Mantilla DE, Misocami MA,    Goncalves SM, Bignelli AT, Riella MC, et al. Effect of preload reduction by    hemodialysis on left atrial volume and echocardiographic Doppler parameters    in patients with end-stage renal disease. Am J Cardiol. 2004; 94: 1208-10.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Effect of preload reduction by hemodialysis on left atrial volume and echocardiographic Doppler parameters in patients with end-stage renal disease</article-title>
          <source>Am J Cardiol</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>1208</fpage>
          <lpage>10</lpage>
          <volume>94</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Mantilla</surname>
              <given-names>DE</given-names>
            </name>
            <name>
              <surname>Misocami</surname>
              <given-names>MA</given-names>
            </name>
            <name>
              <surname>Goncalves</surname>
              <given-names>SM</given-names>
            </name>
            <name>
              <surname>Bignelli</surname>
              <given-names>AT</given-names>
            </name>
            <name>
              <surname>Riella</surname>
              <given-names>MC</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B8">
        <mixed-citation>8. Pecoits-Filho R, Goncalves S, Barberato    SH, Bignelli A, Lindholm B, Riella MC, et al. Impact of residual renal function    on volume status in chronic renal failure. Blood Purif. 2004; 22: 285-92.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Impact of residual renal function on volume status in chronic renal failure</article-title>
          <source>Blood Purif</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>285</fpage>
          <lpage>92</lpage>
          <volume>22</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Pecoits-Filho</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Goncalves</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Bignelli</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Lindholm</surname>
              <given-names>B</given-names>
            </name>
            <name>
              <surname>Riella</surname>
              <given-names>MC</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B9">
        <mixed-citation>9. Devereux RB, Alonso DR, Lutas EM, Gottlieb    GJ, Campo E, Sachs I, et al. Echocardiographic assessment of left ventricular    hypertrophy: comparison to necropsy findings. Am J Cardiol. 1986; 57: 450-8.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings</article-title>
          <source>Am J Cardiol</source>
          <date>
            <year>1986</year>
          </date>
          <fpage>450</fpage>
          <lpage>8</lpage>
          <volume>57</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Devereux</surname>
              <given-names>RB</given-names>
            </name>
            <name>
              <surname>Alonso</surname>
              <given-names>DR</given-names>
            </name>
            <name>
              <surname>Lutas</surname>
              <given-names>EM</given-names>
            </name>
            <name>
              <surname>Gottlieb</surname>
              <given-names>GJ</given-names>
            </name>
            <name>
              <surname>Campo</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Sachs</surname>
              <given-names>I</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B10">
        <mixed-citation>10. de Simone G, Daniels SR, Devereux RB,    Meyer RA, Roman MJ, de Divitiis O, et al. Left ventricular mass and body size    in normotensive children and adults: assessment of allometric relations and    impact of overweight. J Am Coll Cardiol. 1992; 20: 1251-60.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Left ventricular mass and body size in normotensive children and adults: assessment of allometric relations and impact of overweight</article-title>
          <source>J Am Coll Cardiol</source>
          <date>
            <year>1992</year>
          </date>
          <fpage>1251</fpage>
          <lpage>60</lpage>
          <volume>20</volume>
          <person-group person-group-type="author">
            <name>
              <surname>de Simone</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Daniels</surname>
              <given-names>SR</given-names>
            </name>
            <name>
              <surname>Devereux</surname>
              <given-names>RB</given-names>
            </name>
            <name>
              <surname>Meyer</surname>
              <given-names>RA</given-names>
            </name>
            <name>
              <surname>Roman</surname>
              <given-names>MJ</given-names>
            </name>
            <name>
              <surname>de Divitiis</surname>
              <given-names>O</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B11">
        <mixed-citation>11. Lang RM, Bierig M, Devereux RB, Flachskampf    FA, Foster E, Pellikka PA, et al. Recommendations for chamber quantification:    a report from the American Society of Echocardiography's Guidelines and Standards    Committee and the Chamber Quantification Writing Group, developed in conjunction    with the European Association of Echocardiography, a branch of the European    Society of Cardiology. J Am Soc Echocardiogr. 2005; 18: 1440-63.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Recommendations for chamber quantification: a report from the American Society of Echocardiography's Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>1440</fpage>
          <lpage>63</lpage>
          <volume>18</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Lang</surname>
              <given-names>RM</given-names>
            </name>
            <name>
              <surname>Bierig</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Devereux</surname>
              <given-names>RB</given-names>
            </name>
            <name>
              <surname>Flachskampf</surname>
              <given-names>FA</given-names>
            </name>
            <name>
              <surname>Foster</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Pellikka</surname>
              <given-names>PA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B12">
        <mixed-citation>12. Dokainish H, Zoghbi WA, Lakkis NM, Al-Bakshy    F, Dhir M, Quinones MA, et al. Optimal noninvasive assessment of left ventricular    filling pressures: a comparison of tissue Doppler echocardiography and B-type    natriuretic peptide in patients with pulmonary artery catheters. Circulation.    2004; 109: 2432-9.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Optimal noninvasive assessment of left ventricular filling pressures: a comparison of tissue Doppler echocardiography and B-type natriuretic peptide in patients with pulmonary artery catheters</article-title>
          <source>Circulation</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>2432</fpage>
          <lpage>9</lpage>
          <volume>109</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Dokainish</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Zoghbi</surname>
              <given-names>WA</given-names>
            </name>
            <name>
              <surname>Lakkis</surname>
              <given-names>NM</given-names>
            </name>
            <name>
              <surname>Al-Bakshy</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Dhir</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Quinones</surname>
              <given-names>MA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B13">
        <mixed-citation>13. Lester SJ, Tajik AJ, Nishimura RA, Oh    JK, Khandheria BK, Seward JB. Unlocking the mysteries of diastolic function:    deciphering the Rosetta Stone 10 years later. J Am Coll Cardiol. 2008; 51: 679-89.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Unlocking the mysteries of diastolic function: deciphering the Rosetta Stone 10 years later</article-title>
          <source>J Am Coll Cardiol</source>
          <date>
            <year>2008</year>
          </date>
          <fpage>679</fpage>
          <lpage>89</lpage>
          <volume>51</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Lester</surname>
              <given-names>SJ</given-names>
            </name>
            <name>
              <surname>Tajik</surname>
              <given-names>AJ</given-names>
            </name>
            <name>
              <surname>Nishimura</surname>
              <given-names>RA</given-names>
            </name>
            <name>
              <surname>Oh</surname>
              <given-names>JK</given-names>
            </name>
            <name>
              <surname>Khandheria</surname>
              <given-names>BK</given-names>
            </name>
            <name>
              <surname>Seward</surname>
              <given-names>JB</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B14">
        <mixed-citation>14. Barberato SH, Pecoits-Filho R. Usefulness    of left atrial volume for the differentiation of normal from pseudonormal diastolic    function pattern in patients on hemodialysis. J Am Soc Echocardiogr. 2007; 20:    359-65.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Usefulness of left atrial volume for the differentiation of normal from pseudonormal diastolic function pattern in patients on hemodialysis</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>359</fpage>
          <lpage>65</lpage>
          <volume>20</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Pecoits-Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B15">
        <mixed-citation>15. Barberato SH, Pecoits Filho R. Prognostic    value of left atrial volume index in hemodialysis patients. Arq Bras Cardiol.    2007; 88: 643-50.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Prognostic value of left atrial volume index in hemodialysis patients</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>643</fpage>
          <lpage>50</lpage>
          <volume>88</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Pecoits Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B16">
        <mixed-citation>16. Gupta S, Dev V, Kumar MV, Dash SC. Left    ventricular diastolic function in end-stage renal disease and the impact of    hemodialysis. Am J Cardiol. 1993; 71: 1427-30.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Left ventricular diastolic function in end-stage renal disease and the impact of hemodialysis</article-title>
          <source>Am J Cardiol</source>
          <date>
            <year>1993</year>
          </date>
          <fpage>1427</fpage>
          <lpage>30</lpage>
          <volume>71</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Gupta</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Dev</surname>
              <given-names>V</given-names>
            </name>
            <name>
              <surname>Kumar</surname>
              <given-names>MV</given-names>
            </name>
            <name>
              <surname>Dash</surname>
              <given-names>SC</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B17">
        <mixed-citation>17. Foley RN, Parfrey PS, Harnett JD, Kent    GM, Martin CJ, Murray DC, et al. Clinical and echocardiographic disease in patients    starting end-stage renal disease therapy. Kidney Int. 1995; 47: 186-92.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Clinical and echocardiographic disease in patients starting end-stage renal disease therapy</article-title>
          <source>Kidney Int</source>
          <date>
            <year>1995</year>
          </date>
          <fpage>186</fpage>
          <lpage>92</lpage>
          <volume>47</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Foley</surname>
              <given-names>RN</given-names>
            </name>
            <name>
              <surname>Parfrey</surname>
              <given-names>PS</given-names>
            </name>
            <name>
              <surname>Harnett</surname>
              <given-names>JD</given-names>
            </name>
            <name>
              <surname>Kent</surname>
              <given-names>GM</given-names>
            </name>
            <name>
              <surname>Martin</surname>
              <given-names>CJ</given-names>
            </name>
            <name>
              <surname>Murray</surname>
              <given-names>DC</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B18">
        <mixed-citation>18. Mall G, Huther W, Schneider J, Lundin    P, Ritz E. Diffuse intermyocardiocytic fibrosis in uraemic patients. Nephrol    Dial Transplant. 1990; 5: 39-44.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Diffuse intermyocardiocytic fibrosis in uraemic patients</article-title>
          <source>Nephrol Dial Transplant</source>
          <date>
            <year>1990</year>
          </date>
          <fpage>39</fpage>
          <lpage>44</lpage>
          <volume>5</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Mall</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Huther</surname>
              <given-names>W</given-names>
            </name>
            <name>
              <surname>Schneider</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Lundin</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Ritz</surname>
              <given-names>E</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B19">
        <mixed-citation>19. Ritz E, Rambausek M, Mall G, Ruffmann    K, Mandelbaum A. Cardiac changes in uraemia and their possible relationship    to cardiovascular instability on dialysis. Nephrol Dial Transplant. 1990; 5    (Suppl 1): 93-7.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Cardiac changes in uraemia and their possible relationship to cardiovascular instability on dialysis</article-title>
          <source>Nephrol Dial Transplant</source>
          <date>
            <year>1990</year>
          </date>
          <fpage>93</fpage>
          <lpage>7</lpage>
          <volume>5</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ritz</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Rambausek</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Mall</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Ruffmann</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Mandelbaum</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B20">
        <mixed-citation>20. Ommen SR, Nishimura RA, Appleton CP, Miller    FA, Oh JK, Redfield MM, et al. Clinical utility of Doppler echocardiography    and tissue Doppler imaging in the estimation of left ventricular filling pressures:    a comparative simultaneous Doppler-catheterization study. Circulation. 2000;    102: 1788-94.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Clinical utility of Doppler echocardiography and tissue Doppler imaging in the estimation of left ventricular filling pressures: a comparative simultaneous Doppler-catheterization study</article-title>
          <source>Circulation</source>
          <date>
            <year>2000</year>
          </date>
          <fpage>1788</fpage>
          <lpage>94</lpage>
          <volume>102</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ommen</surname>
              <given-names>SR</given-names>
            </name>
            <name>
              <surname>Nishimura</surname>
              <given-names>RA</given-names>
            </name>
            <name>
              <surname>Appleton</surname>
              <given-names>CP</given-names>
            </name>
            <name>
              <surname>Miller</surname>
              <given-names>FA</given-names>
            </name>
            <name>
              <surname>Oh</surname>
              <given-names>JK</given-names>
            </name>
            <name>
              <surname>Redfield</surname>
              <given-names>MM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B21">
        <mixed-citation>21. Sharma R, Pellerin D, Gaze DC, Mehta RL,    Gregson H, Streather CP, et al. Mitral peak Doppler E-wave to peak mitral annulus    velocity ratio is an accurate estimate of left ventricular filling pressure    and predicts mortality in end-stage renal disease. J Am Soc Echocardiogr. 2006;    19: 266-73.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Mitral peak Doppler E-wave to peak mitral annulus velocity ratio is an accurate estimate of left ventricular filling pressure and predicts mortality in end-stage renal disease</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2006</year>
          </date>
          <fpage>266</fpage>
          <lpage>73</lpage>
          <volume>19</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Sharma</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Pellerin</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Gaze</surname>
              <given-names>DC</given-names>
            </name>
            <name>
              <surname>Mehta</surname>
              <given-names>RL</given-names>
            </name>
            <name>
              <surname>Gregson</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Streather</surname>
              <given-names>CP</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B22">
        <mixed-citation>22. Wang AY, Wang M, Lam CW, Chan IH, Zhang    Y, Sanderson JE. Left ventricular filling pressure by Doppler echocardiography    in patients with end-stage renal disease. Hypertension. 2008; 52: 107-14.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Left ventricular filling pressure by Doppler echocardiography in patients with end-stage renal disease</article-title>
          <source>Hypertension</source>
          <date>
            <year>2008</year>
          </date>
          <fpage>107</fpage>
          <lpage>14</lpage>
          <volume>52</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Wang</surname>
              <given-names>AY</given-names>
            </name>
            <name>
              <surname>Wang</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Lam</surname>
              <given-names>CW</given-names>
            </name>
            <name>
              <surname>Chan</surname>
              <given-names>IH</given-names>
            </name>
            <name>
              <surname>Zhang</surname>
              <given-names>Y</given-names>
            </name>
            <name>
              <surname>Sanderson</surname>
              <given-names>JE</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B23">
        <mixed-citation>23. Barberato SH, Misocami MA, Pecoits-Filho    R. Association between left atrium enlargement and intradialytic hypotension:    role of diastolic dysfunction in the hemodynamic complications during hemodialysis.    Echocardiography. 2009. [In press]</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Association between left atrium enlargement and intradialytic hypotension: role of diastolic dysfunction in the hemodynamic complications during hemodialysis</article-title>
          <source>Echocardiography</source>
          <date>
            <year>2009</year>
          </date>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Misocami</surname>
              <given-names>MA</given-names>
            </name>
            <name>
              <surname>Pecoits-Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
    </ref-list>
  </back>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Articles</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Prevalence and prognostic impact of diastolic dysfunction in patients with chronic kidney disease on hemodialysis</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: Diastolic dysfunction (DD) is frequent in patients on hemodialysis (HD), but its impact on the clinical evolution is yet to be established. OBJECTIVE: To evaluate the prevalence and prognostic impact of left ventricular (LV) advanced diastolic dysfunction (ADD) in patients on hemodialysis. METHODS: The echocardiograms were performed during the first year of HD therapy, in patients with sinus rhythm, with no evidence of cardiovascular disease, excluding those with significant valvopathy or pericardial effusion. The combined assessment of the Doppler echocardiographic data classified the diastolic dysfunction as: 1) normal diastolic function; 2) mild DD (relaxation alteration) and 3) ADD (pseudonormalization and restrictive flow pattern). The assessed outcomes were general mortality and cardiovascular events. RESULTS: A total of 129 patients (78 males), aged 52 &#177; 16 years, with a DD prevalence of 73% (50% with mild DD and 23% with ADD) were included in the study. The group with ADD was older (p &lt; 0.01) and presented higher systolic (p &lt; 0.01) and diastolic BP (p = 0.043), LV mass (p &lt; 0.01), left atrial volume index (p &lt; 0.01) and number of diabetic patients (p = 0.019), as well as lower ejection fraction (EF) (p &lt; 0.01). After 17 &#177; 7 months, the general mortality was significantly higher in individuals with ADD, when compared to those with normal function and mild DD (p = 0.012, log rank test). At Cox multivariate analysis, ADD was predictive of cardiovascular events (hazard ratio 2.2; confidence interval: 1.1-4.3; p = 0.021) after adjusted for age, gender, diabetes, LV mass and EF. CONCLUSION: The subclinical ADD was identified in approximately 25% of the patients undergoing hemodialysis and had a prognostic impact, regardless of other clinical and echocardiographic data.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Kidney diseases</kwd>
        <kwd>renal dialysis</kwd>
        <kwd>ventricular dysfunction, left</kwd>
        <kwd>ventricular dysfunction, left</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ORIGINAL ARTICLE</bold>
      </p>
      <p><undefined id="linkinicio-body2"/>Prevalence and prognostic impact of diastolic dysfunction in patients with chronic Kidney disease on hemodialysis</p>
      <p>
        <bold>Silvio H. Barberato<sup>I,II</sup>; S&#233;rgio G. E. Bucharles<sup>I</sup>; Admar M. Sousa<sup>II</sup>; Costantino O. Costantini<sup>II</sup>; Costantino R. F. Costantini<sup>II</sup>; Roberto Pecoits-Filho<sup>I</sup></bold>
      </p>
      <p><sup>I</sup>Pontif&#237;cia Universidade Cat&#243;lica do Paran&#225;</p>
      <p><sup>II</sup>Hospital Cardiol&#243;gico Costantini, Curitiba, PR - Brazil</p>
      <p>Mailing address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>BACKGROUND:</bold> Diastolic dysfunction (DD) is frequent in patients on hemodialysis (HD), but its impact on the clinical evolution is yet to be established.</p>
      <p><bold>OBJECTIVE:</bold> To evaluate the prevalence and prognostic impact of left ventricular (LV) advanced diastolic dysfunction (ADD) in patients on hemodialysis.</p>
      <p><bold>METHODS:</bold> The echocardiograms were performed during the first year of HD therapy, in patients with sinus rhythm, with no evidence of cardiovascular disease, excluding those with significant valvopathy or pericardial effusion. The combined assessment of the Doppler echocardiographic data classified the diastolic dysfunction as: 1) normal diastolic function; 2) mild DD (relaxation alteration) and 3) ADD (pseudonormalization and restrictive flow pattern). The assessed outcomes were general mortality and cardiovascular events.</p>
      <p><bold>RESULTS:</bold> A total of 129 patients (78 males), aged 52 &#177; 16 years, with a DD prevalence of 73% (50% with mild DD and 23% with ADD) were included in the study. The group with ADD was older (p &lt; 0.01) and presented higher systolic (p &lt; 0.01) and diastolic BP (p = 0.043), LV mass (p &lt; 0.01), left atrial volume index (p &lt; 0.01) and number of diabetic patients (p = 0.019), as well as lower ejection fraction (EF) (p &lt; 0.01). After 17 &#177; 7 months, the general mortality was significantly higher in individuals with ADD, when compared to those with normal function and mild DD (p = 0.012, log rank test). At Cox multivariate analysis, ADD was predictive of cardiovascular events (hazard ratio 2.2; confidence interval: 1.1-4.3; p = 0.021) after adjusted for age, gender, diabetes, LV mass and EF.</p>
      <p><bold>CONCLUSION:</bold> The subclinical ADD was identified in approximately 25% of the patients undergoing hemodialysis and had a prognostic impact, regardless of other clinical and echocardiographic data. (Arq Bras Cardiol 2010; 94(4):431-436)</p>
      <p><bold>Key words:</bold> Kidney diseases; renal dialysis; ventricular dysfunction, left/physiopathology/therapeutic.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Cardiovascular complications are the main cause of death in patients with chronic kidney disease (CKD) undergoing renal replacement therapy through hemodialysis (HD)<sup>1</sup>.</p>
      <p>In these individuals, the finding of left ventricular (LV) echocardiographic alterations, such as LV hypertrophy, dilation and systolic dysfunction, results in a 3-fold higher risk of heart failure, regardless of age, diabetes and coronary failure<sup>2</sup>. On the other hand, although the LV filling alterations are often detected in this group, the actual prevalence of diastolic dysfunction (DD) and its impact on the clinical evolution are yet to be established<sup>3,4</sup>. </p>
      <p>From the hemodynamic point of view, the increase in the left intraventricular diastolic pressure is the phenomenon responsible for the onset of heart failure, whatever the underlying cause is<sup>5</sup>. Therefore, it becomes important to detect the presence of advanced DD (ADD), characterized by the increase in the filling pressures, especially at the subclinical phase.</p>
      <p>In this context, the Doppler echocardiographic pre-load independent techniques, such as tissue Doppler<sup>6</sup> and left atrial volume<sup>7</sup>, represent an important advancement in the assessment of diastolic function.</p>
      <p>The objectives of the present study are to estimate the prevalence, identify predisposing factors and evaluate the prognostic impact of left ventricular ADD in individuals on HD with no clinical evidence of cardiovascular disease.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>
        <bold>Population</bold>
      </p>
      <p>Patients eligible for the study were those with chronic kidney disease (CKD) undergoing maintenance hemodialysis (4-hour sessions, three times a week), at two Services of Nephrology in University hospitals.</p>
      <p>The inclusion criteria were: to have been undergoing HD for a period between 1 and 12 months, no previous cardiovascular diseases (congestive heart failure, acute myocardial infarction, cerebrovascular accident or peripheral arterial failure) and sign the free and informed consent form. The exclusion criteria were: malignant diseases, active infection, non-sinus rhythm, significant valvopathy (valve prosthesis, any degree of mitral or aortic stenosis and moderate to significant mitral, aortic or tricuspid regurgitation), pericardial effusion, and technically unsatisfactory echocardiogram. All patients were submitted to HD in an Altra Touch equipment (Althin, Miami, Florida, Fl, USA) , containing a cellulose acetate dialyzer with a minimum blood flow regulation of 200 ml/minute and dialysate flow of 300 to 500 ml/minute. The "dry-weight" estimation (volume to be removed by ultrafiltration) was carried out by clinical signs of hydration, blood pressure behavior during the HD session and electrical bioimpedance<sup>8</sup>. The body surface was calculated using the equation proposed by Du Bois and Du Bois (0.20247 x weight<sup>0.425 </sup>x height<sup>0.725</sup>). The body mass index (BMI) was calculated by dividing the weight in kilograms by the height in meters squared; obesity was considered when BMI &gt; 30. The systolic and diastolic arterial pressures, heart rate, weight and height were measured at the time of the assessment. The Ethical Committee in Research of our institution approved the study protocol and informed consent was obtained from all patients.</p>
      <p>
        <bold>Doppler echocardiogram</bold>
      </p>
      <p>The assessments were carried out on interdialytic days, between 12 PM and 6 PM. The patients were placed on left lateral decubitus, using an Envisor C echocardiographic equipment (Phillips Inc., Andover, Massachusetts, EUA) equipped with 2 to 4 MHz transducers to undergo the complete echocardiographic assessment through the M-mode, two-dimensional and Doppler techniques (pulsed, continuous, color and tissue). </p>
      <p>The following parameters were obtained in the M-mode: anteroposterior diameter of the left atrium, thickness of the interventricular septum and LV posterior wall in diastole, LV-end diastolic diameter (dilatation when &gt; 54 mm for women and &gt; 56 mm for men) and LV-end systolic diameter. LV mass was estimated using Devereux equation<sup>9</sup> and index by height to the power of 2.7<sup>10</sup>. LV hypertrophy was defined as the presence of mass/height<sup>2.7</sup><underline>&gt;</underline> 45 g/m<sup>2.7</sup> for women and <underline>&gt;</underline> 49 g/m<sup>2.7 </sup>for men<sup>11</sup>. Systolic function was assessed by calculating ejection fraction (EF) using Simpson's method<sup>11</sup>. Mitral transvalvular flow was recorded in 4-chamber apical view with the pulsed Doppler sampling positioned between the extremities of the mitral cusps, and we measured the early filling velocity (E wave), atrial contraction velocity (A wave) and E/A ratio. The tissue Doppler velocities were recorded in the 4-chamber apical view with a volume sampling positioned consecutively on the junction between the LV lateral and septal walls with the mitral annulus<sup>12</sup>. The early (E') and late (A') diastolic mitral annular velocities were analyzed and the E'/A' and E/E' (average of septal and lateral annulus sides) ratios were calculated. The left atrial volume was determined at the two-dimensional Doppler using Simpson's biplane technique<sup>11</sup> and indexed for body surface. A total of three cardiac cycles were considered for all measurements.</p>
      <p>
        <bold>Diastolic function assessment</bold>
      </p>
      <p>LV diastolic function was classified by considering the interpretation of all conventional and tissue-Doppler derived indices of the mitral annulus in four patterns: normal, relaxation alteration (E/A ratio &lt; 1 and E' &lt; 10 cm/s), pseudonormal and restrictive flow pattern ( E/A ratio &gt; 2 and E' &lt; 8 cm/s)<sup>13</sup>. The diagnosis of the pseudonormal pattern (differentiating it from the actual normal one) used the following criteria: E/E' ratio &gt; 15<sup>13</sup>; or b) E/E' ratio <underline>&gt;</underline> 11<sup>12</sup>,associated to a left atrial volume index &gt; 35 ml/m<sup>2,14</sup>. The sample was subsequently classified in three groups, according to the hemodynamic pattern of LV filling: 1) normal diastolic function, 2) mild DD (MDD) (relaxation alteration) and 3) ADD (comprehending restrictive flow and pseudonormalization).</p>
      <p>
        <bold>Analysis of survival</bold>
      </p>
      <p>Demographic data, comorbidities (diabetes mellitus, arterial hypertension, dyslipidemia, smoking), current medications and routine laboratory findings were obtained after a careful analysis of the patients' files, in addition to an interview with the physician in charge of the patient's treatment, when necessary. The primary and secondary outcomes were, respectively, general mortality and a combination of fatal and nonfatal cardiovascular events. The analyzed events were cardiovascular death (including sudden death, acute myocardial infarction, cerebrovascular accident), nonfatal myocardial infarction and decompensated congestive heart failure (requiring hospitalization). The follow-up was based on the analysis of the outcomes, periodically performed at the dialysis clinic. Patients submitted to kidney transplant or that changed the type of dialysis were censored.</p>
      <p>
        <bold>Statistical analysis</bold>
      </p>
      <p>An adequate descriptive analysis was applied to continuous (means and standard deviations) and categorical (percentages) variables. Comparisons between the groups were carried out by analysis of variance (ANOVA), with Dunnett's post hoc correction for continuous variables and Chi-square test for categorical variables. The logistic regression analysis determined the independent predictors of DD. Kaplan-Meier survival curves for the diastolic function status were constructed and compared by the log-rank test. The independent prognostic impact of DD was evaluated by the multivariate analysis of survival using Cox's model, considering established risk predictors in this population. The level of statistical significance was set at p &lt; 0.05. The SPSS 13 for Windows and JMP IN 5.1 statistical packages were used for all statistical analyses.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>
        <bold>Basal characteristics</bold>
      </p>
      <p>The demographic, clinical, biochemical and Doppler echocardiographic characteristics of the 129 patients that formed the study population are shown in <xref ref-type="table" rid="tab01-body2">Table 1</xref>. The group consisted of 78 men and 51 women, with a mean age of 52 &#177; 16 years and time of dialysis of 7 &#177; 4 months. The etiology of the CKD was attributed to hypertensive nephrosclerosis (39%), diabetic nephropathy (21%), an association of the former two (15%), chronic glomerulonephritis (14%), polycystic kidney (5%), lithiasis (3%), chronic pyelonephritis (2%) and other diseases (1%). Most patients (77%) used anti-hypertensive medications, especially angiotensin-converting enzyme inhibitors (46%), beta-blockers (16%), alpha-blockers (13%), calcium-channel antagonists (12%) and angiotensin-receptor blockers (11%), either alone or in combination.</p>
      <table-wrap id="tab01-body2">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt01-en.jpg"/></table-wrap>
      <p>
        <bold>Clinical and doppler echocardiographic alterations</bold>
      </p>
      <p>At the study enrollment, 45% of the patients had arterial hypertension, 34% had diabetes mellitus, 25% had dyslipidemia and 11% were smokers. The prevalence of obesity (BMI &gt; 30) was 9%. LV dilatation was present in 34 patients (26%), LV hypertrophy in 110 (85%) and systolic dysfunction in 24 patients (19%), either alone or in combination. Only 19 patients (15%) presented normal LV dimensions. Significant left atrial dilatation (volume &gt; 32 ml/m<sup>2</sup>) was observed in 58 individuals (45%).</p>
      <p>
        <bold>Prevalence of diastolic dysfunction</bold>
      </p>
      <p>DD was diagnosed in 94 of the 129 patients (73%), with 64 presenting mild DD - MDD (50%) and 30 advanced DD - ADD (23%). In the ADD group, 20 patients presented flow pseudonormalization and 10 presented restrictive flow. In parallel, only 22 patients (17%) presented a mean E/E' ratio &gt; 15. When considering solely the conventional Doppler data, only 80 (62%) of the 129 studied patients would have been diagnosed with DD.</p>
      <p>
        <bold>Predictors of advanced DD</bold>
      </p>
      <p>The main differences between the groups with normal diastolic function, mild DD and advanced DD are shown in <xref ref-type="table" rid="tab02-body2">Table 2</xref>. The group of individuals with ADD was older (p &lt; 0.01), had higher systolic arterial pressure (p &lt; 0.01), diastolic arterial pressure (0.043), LV mass (p &lt; 0.01) and left atrial volume index (p &lt; 0.01), as well as a higher proportion of diabetics (p = 0.019) and a lower ejection fraction (p &lt; 0.01). After the multivariate logistic regression analysis, using the group with normal function as control, the independent predictors of ADD were diabetes (odds ratio [OR]: 2; CI: 1.6-5.9, p = 0.011), systolic arterial pressure (OR 1.05; CI: 1.01-1.09, p = 0.023) and LV mass (OR 1.06; CI: 1.01-1.1, p &lt; 0.01), in addition to a tendency for the ejection fraction (p = 0.052).</p>
      <table-wrap id="tab02-body2">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt02-en.jpg"/></table-wrap>
      <p>
        <bold>Outcomes</bold>
      </p>
      <p>During the mean follow-up of 17 &#177; 7 months, there were 26 deaths (20%) and 21 nonfatal cardiovascular events (16%). The deaths were attributed to cardiovascular (18 deaths, with 8 due to myocardial infarction, 7 due to sudden death, 2 due to documented complex ventricular arrhythmia and 1 due to hemorrhagic cerebrovascular accident) and infectious causes (8 deaths). The nonfatal cardiovascular events were myocardial infarction (5) and hospitalizations due to decompensated heart failure (16), totaling 39 combined cardiovascular events. As shown in <xref ref-type="fig" rid="fig01-body2">Figure 1</xref> and <xref ref-type="table" rid="tab03-body2">Table 3</xref>, the general mortality was higher in the group with advanced DD (37%) in comparison to the groups with normal and mild DD (9% and 19%, respectively, log rank test, p = 0.012). Several analyses were carried out using Cox multivariate models. After the evaluation of general mortality and cardiovascular events separately (models including age, male sex, diabetes, LV mass and EF), LV mass and EF showed to be independent predictors for both outcomes, in addition to age for cardiovascular events, only. The inclusion of advanced DD in these models reached a statistically significant value for the prediction of cardiovascular events (hazard ratio [HR] 2.2; CI: 1.1-4.3, p = 0.021) and a borderline value for general mortality (HR 2.8; CI: 0.97-8.2, p = 0.056), as seen in <xref ref-type="table" rid="en_a05tab04-body2">Table 4</xref>. In contrast, there was no difference regarding the outcomes between patients with and without E/E' ratio &gt; 15 or E'&lt; 8 cm/s. At an alternative analysis, advanced DD and left atrial volume index (recently described as a prognostic predictor in patients undergoing HD<sup>15</sup>) were included together at the last step of the model. Both advanced DD (HR: 3.4; CI: 1.3-9.2, p = 0.03) and left atrial volume index (HR: 6.6; CI: 1.8-24, p = 0.004) were predictive of cardiovascular events.</p>
      <p content-type="asset">
        <table-wrap id="en_a05tab04-body2">
          <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt03-en.jpg"/></table-wrap>
      </p>
      <fig id="fig01-body2">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gf01-en.jpg"/></fig>
      <table-wrap id="tab03-body2">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt04-en.jpg"/></table-wrap>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>The present study suggests that almost 75% of the individuals undergoing the first year of HD present DD and that approximately 25% of them present ADD. Studies with smaller samples reported DD incidence in 50-65% of uremic patients, including pre-dialysis populations, those undergoing dialysis and post-transplant populations<sup>4</sup> (a percentage similar to that found in our group, if the tissue Doppler and left atrial volume data were not taken into account). Such analyses were limited by the use of transmitral flow-derived parameters and those derived from the pulmonary venous flow to categorize diastolic function<sup>16</sup>. It is known that such methods are particularly vulnerable to preload variations<sup>6</sup>; therefore, such approach might have induced false-negative results, diagnosing individuals with pseudonormalization (high filling pressures "masking" the LV relaxation alteration) as normal. In this context, to combine the conventional Doppler data with techniques that are relatively independent from the preload, such as the tissue Doppler and left atrial volume adds accuracy to the diagnosis of DD and especially of the ADD, characterized by high diastolic intraventricular pressure.</p>
      <p>To detect the presence of DD and estimate the LV filling pressures is currently of general interest to predict the risk of developing the so-called "heart failure with preserved ejection fraction". The clinically evident heart failure represents an independent predictor of mortality in patients starting hemodialysis therapy<sup>17</sup>, but the identification of the underlying cause can be important to direct the therapeutic management. Necropsy and experimental uremia studies have pointed out the presence of specific diffuse intermyocardiocytic fibrosis in the heart of uremic individuals, which could predispose to electrical instability (associated with sudden death) and an increase in filling pressures<sup>18,19</sup>.</p>
      <p>The effect on the physiopathological mechanisms related to marked myocardial fibrosis, such as the activation of humoral factors (plasma angiotensin II, parathyroid hormone, endothelin, aldosterone and catecholamines)<sup>3</sup>, can represent an important therapeutic target, especially at the subclinical phase. </p>
      <p>In spite of such considerations, whether the diagnosis of ADD collaborates to refine and stratify the cardiovascular risk in uremic patients has been little investigated. Recently, two studies tried to estimate the prognostic impact of ADD on CKD through the E/E' ratio, an acknowledged noninvasive index of LV filling pressures in the general population<sup>12,20</sup>. In a study with 125 candidates to kidney transplant, Sharma et al<sup>21</sup> found an association between E/E' &gt; 15 and higher general mortality. However, the study population was heterogeneous (only one-third of the patients was undergoing HD) and only the univariate analysis was performed, which did not allow inferring whether E/E' ratio adds a prognostic value to the traditional assessment of cardiovascular risk in this group. </p>
      <p>Wang et al<sup>22</sup> reported, in a study with 220 patients (exclusively undergoing peritoneal dialysis), that E/E' &gt; 15 was able to predict general and cardiac mortality better than the classic clinical and echocardiographic data. In our population, which consisted exclusively of patients undergoing HD, the E/E' ratio &gt; 15 did not present a discriminating power regarding the studied outcomes. The physiopathology of the cardiovascular disease in individuals undergoing HD is influenced by the abrupt and extensive volemic variations to which these patients are submitted<sup>23</sup>. </p>
      <p>The accurate prediction of the filling pressures (and, consequently, of the prognosis) for a certain individual requires the inclusion of all available data, which makes the approach more consistent than a single parameter considered alone.</p>
      <p> Among the study limitations, it is important to mention the relatively small sample size, which was compensated, however, by the attained statistical power (86% for the primary outcome and 94% for the secondary one). Other limitations were the absence of invasive measurements of LV filling pressure (practical and ethical questions would not justify a cardiac catheterism in the studied population) and the stringent exclusion criteria (which might have made our findings not applicable to all of the dialyzed population).</p>
      <p>
        <bold>Conclusions</bold>
      </p>
      <p>The present study indicates that ADD, diagnosed through the combined interpretation of Doppler echocardiographic information, has a prognostic impact on dialyzed patients with no previous history of cardiovascular events.</p>
      <p>The general mortality was significantly higher in the group with ADD, when compared to those with normal diastolic function and mild DD. In parallel, the ADD was predictive of cardiovascular events, regardless of age, gender, diabetes, LV mass and ejection fraction.</p>
      <p>
        <bold>Potential Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article was reported.</p>
      <p>
        <bold>Sources of Funding</bold>
      </p>
      <p>The present study was partially supported by a cardiology research grant from Brazilian Society of Cardiology.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This study is not associated with any post-graduation program.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
  <sub-article article-type="translation" id="TRes" xml:lang="es">
    <front-stub>
      <article-categories/>
      <title-group>
        <article-title xml:lang="es">Prevalencia e impacto pron&#243;stico de la disfunci&#243;n diast&#243;lica en la enfermedad renal cr&#243;nica en hemodi&#225;lisis</article-title>
      </title-group>
      <abstract xml:lang="es">
        <p>FUNDAMENTO: Disfunci&#243;n diast&#243;lica es frecuente en pacientes de hemodi&#225;lisis, pero su impacto en la evoluci&#243;n cl&#237;nica es incierto. OBJETIVO: Evaluar la prevalencia y el impacto pron&#243;stico de la disfunci&#243;n diast&#243;lica (DD) avanzada (DDA) del ventr&#237;culo izquierdo (VI) en pacientes de hemodi&#225;lisis. M&#201;TODOS: Se realizaron ecocardiogramas en pacientes en el primer a&#241;o de hemodi&#225;lisis, en ritmo sinusal, sin enfermedad cardiovascular manifestada, excluy&#233;ndose aquellos con valvulopat&#237;a significativa o derrame peric&#225;rdico. Por la evaluaci&#243;n integrada de los datos del ecocardiograma Doppler, la funci&#243;n diast&#243;lica fue clasificada como: 1) normal, 2) DD discreta (alteraci&#243;n de la relajaci&#243;n) y 3) DDA (seudonormalizaci&#243;n y flujo restrictivo). Los desenlaces investigados fueron mortalidad general y eventos cardiovasculares. RESULTADOS: Fueron incluidos 129 pacientes (78 hombres), con edad 52 &#177; 16 a&#241;os y prevalencia de DD del 73% (50% con DD discreta y 23% con DDA). En el grupo con DDA, se present&#243; mayor edad (p &lt; 0,01), presi&#243;n arterial sist&#243;lica (p &lt; 0,01) y diast&#243;lica (p = 0,043), masa del VI (p &lt; 0,01), &#237;ndice del volumen del atrio izquierdo (p &lt; 0,01) y proporci&#243;n de diab&#233;ticos (p = 0,019), adem&#225;s de menor fracci&#243;n de eyecci&#243;n (p &lt; 0,01). Despu&#233;s de 17 &#177; 7 meses, la mortalidad general fue significativamente mayor en aquellos con DDa, en comparaci&#243;n a los normales y con DD discreta (p = 0,012, log rank test). En el an&#225;lisis multivariado de Cox, la DDA fue predictiva de eventos cardiovasculares (hazard ratio 2,2, intervalo de confianza 1,1-4,3, p = 0,021) despu&#233;s del ajuste para edad, sexo, diabetes, masa del VI y fracci&#243;n de eyecci&#243;n. CONCLUSI&#211;N: La DDA subl&#237;nica se encontr&#243; en aproximadamente un cuarto de los pacientes de hemodi&#225;lisis y result&#243; de impacto pron&#243;stico, independiente de otros datos cl&#237;nicos y ecocardiogr&#225;ficos.</p>
      </abstract>
      <kwd-group xml:lang="es">
        <kwd>Enfermedades renales</kwd>
        <kwd>di&#225;lisis renal</kwd>
        <kwd>disfunci&#243;n del ventr&#237;culo izquierdo</kwd>
        <kwd>disfunci&#243;n del ventr&#237;culo izquierdo</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ART&#205;CULO ORIGINAL</bold>
      </p>
      <p>
        <fn id="top-body3">
          <label>
            <bold>Prevalencia e impacto pron&#243;stico de la disfunci&#243;n diast&#243;lica en la enfermedad renal cr&#243;nica en hemodi&#225;lisis</bold>
          </label>
          <p>
            <bold>Silvio H. Barberato<sup>I, II</sup>; S&#233;rgio G. E. Bucharles<sup>I</sup>; Admar M. Sousa<sup>II</sup>; Costantino O. Costantini<sup>II</sup>; Costantino R. F. Costantini<sup>II</sup>; Roberto Pecoits-Filho<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Pontif&#237;cia Universidade Cat&#243;lica do Paran&#225;</p>
      <p><sup>II</sup>Hospital Cardiol&#243;gico Costantini, Curitiba, PR - Brasil</p>
      <p>Correspondencia</p>
      <p>
        <bold>RESUMEN</bold>
      </p>
      <p><bold>FUNDAMENTO: </bold> Disfunci&#243;n diast&#243;lica es frecuente en pacientes de hemodi&#225;lisis, pero su impacto en la evoluci&#243;n cl&#237;nica es incierto.</p>
      <p> OBJETIVO: Evaluar la prevalencia y el impacto pron&#243;stico de la disfunci&#243;n diast&#243;lica (DD) avanzada (DDA) del ventr&#237;culo izquierdo (VI) en pacientes de hemodi&#225;lisis.</p>
      <p><bold>M&#201;TODOS: </bold> Se realizaron ecocardiogramas en pacientes en el primer a&#241;o de hemodi&#225;lisis, en ritmo sinusal, sin enfermedad cardiovascular manifestada, excluy&#233;ndose aquellos con valvulopat&#237;a significativa o derrame peric&#225;rdico. Por la evaluaci&#243;n integrada de los datos del ecocardiograma Doppler, la funci&#243;n diast&#243;lica fue clasificada como: 1) normal, 2) DD discreta (alteraci&#243;n de la relajaci&#243;n) y 3) DDA (seudonormalizaci&#243;n y flujo restrictivo). Los desenlaces investigados fueron mortalidad general y eventos cardiovasculares.</p>
      <p><bold>RESULTADOS: </bold> Fueron incluidos 129 pacientes (78 hombres), con edad 52 &#177; 16 a&#241;os y prevalencia de DD del 73% (50% con DD discreta y 23% con DDA). En el grupo con DDA, se present&#243; mayor edad (p &lt; 0,01), presi&#243;n arterial sist&#243;lica (p &lt; 0,01) y diast&#243;lica (p = 0,043), masa del VI (p &lt; 0,01), &#237;ndice del volumen del atrio izquierdo (p &lt; 0,01) y proporci&#243;n de diab&#233;ticos (p = 0,019), adem&#225;s de menor fracci&#243;n de eyecci&#243;n (p &lt; 0,01). Despu&#233;s de 17 &#177; 7 meses, la mortalidad general fue significativamente mayor en aquellos con DDa, en comparaci&#243;n a los normales y con DD discreta (p = 0,012, <italic>log rank test</italic>). En el an&#225;lisis multivariado de Cox, la DDA fue predictiva de eventos cardiovasculares (<italic>hazard ratio</italic> 2,2, intervalo de confianza 1,1-4,3, p = 0,021) despu&#233;s del ajuste para edad, sexo, diabetes, masa del VI y fracci&#243;n de eyecci&#243;n.</p>
      <p><bold>CONCLUSI&#211;N: </bold> La DDA subl&#237;nica se encontr&#243; en aproximadamente un cuarto de los pacientes de hemodi&#225;lisis y result&#243; de impacto pron&#243;stico, independiente de otros datos cl&#237;nicos y ecocardiogr&#225;ficos.</p>
      <p><bold>Palabras clave: </bold> Enfermedades renales, di&#225;lisis renal, disfunci&#243;n del ventr&#237;culo izquierdo/fisiopatolog&#237;a/terapia.</p>
      <p>
        <bold>Introducci&#243;n</bold>
      </p>
      <p>Las complicaciones cardiovasculares son las principales causas de fallecimiento en los pacientes portadores de enfermedad renal cr&#243;nica (ERC) en terapia de sustituci&#243;n renal por hemodi&#225;lisis (HD)<sup>1</sup>. En estos individuos, el hallazgo de alteraciones ecocardiogr&#225;ficas del ventr&#237;culo izquierdo (VI), como hipertrofia, dilataci&#243;n y disfunci&#243;n sist&#243;lica, triplica el riesgo de insuficiencia card&#237;aca, independiente de edad, diabetes e insuficiencia coronaria<sup>2</sup>. Por otro lado, aunque las alteraciones del llenado ventricular izquierdo sean frecuentemente detectadas en ese grupo, la prevalencia real de la disfunci&#243;n diast&#243;lica (DD) y su impacto en la evoluci&#243;n cl&#237;nica no son conocidos<sup>3,4</sup>. Desde el punto de vista hemodin&#225;mico, la elevaci&#243;n de la presi&#243;n diast&#243;lica intraventricular izquierda es el fen&#243;meno responsable por la manifestaci&#243;n de la insuficiencia card&#237;aca, cualquiera sea la causa subyacente<sup>5</sup>. Por lo tanto, resulta oportuno detectar la presencia de la DD avanzada (DDA), caracterizada por el aumento de las presiones de llenado, sobre todo en la fase subcl&#237;nica. En este contexto, t&#233;cnicas de ecocardiograma Doppler relativamente independientes de la precarga, como el Doppler tisular<sup>6</sup> y el volumen del atrio izquierdo<sup>7</sup>, representan un importante avanzo en la evaluaci&#243;n de la funci&#243;n diast&#243;lica. Los objetivos de este estudio son estimar la prevalencia, identificar factores predisponentes y evaluar el impacto pron&#243;stico de la DDA del VI en individuos iniciando HD sin enfermedad cardiovascular cl&#237;nicamente manifiesta.</p>
      <p>
        <bold>M&#233;todos</bold>
      </p>
      <p>
        <bold>Poblaci&#243;n</bold>
      </p>
      <p>Fueron considerados elegibles para el estudio pacientes portadores de ERC que estaban en programa de HD de mantenimiento (sesiones con duraci&#243;n de 4 horas, tres veces por semana) en dos servicios de nefrolog&#237;a basados en hospitales universitarios. Los criterios de inclusi&#243;n fueron: estar en terapia hemodial&#237;tica entre uno y 12 meses, ausencia de afecciones cardiovasculares anteriores (insuficiencia card&#237;aca congestiva, infarto agudo de miocardio, accidente vascular cerebral o insuficiencia arterial perif&#233;rica) y firma del t&#233;rmino de consentimiento. Los criterios de exclusi&#243;n fueron: malignidades, infecci&#243;n activa, ritmo card&#237;aco no sinusal, valvulopat&#237;a significativa (pr&#243;tesis valvular, cualquier grado de estenosis mitral o a&#243;rtica, e insuficiencia mitral, a&#243;rtica o tric&#250;spide moderada a importante), derrame peric&#225;rdico y ecocardiograma t&#233;cnicamente insatisfactorio. Todos los pacientes fueron sometidos a di&#225;lisis con m&#225;quinas Altra Touch (Althin, Miami, Florida, Fl, EEUU) conteniendo dializador de acetato de celulosa regulado con flujo de sangre m&#237;nimo de 200 ml/minuto y flujo de dializado de 300-500 ml/minuto. La estimativa de "peso seco" (volumen a ser retirado por ultrafiltraci&#243;n) fue realizada por medio de se&#241;ales cl&#237;nicas de hidrataci&#243;n, comportamiento de la presi&#243;n arterial durante la sesi&#243;n y bioimpedancia el&#233;ctrica<sup>8</sup>. La superficie corp&#243;rea se calcul&#243; de acuerdo con la ecuaci&#243;n de Du Bois y Du Bois (0,20247 x peso<sup>0,425</sup> x altura<sup>0,725</sup>). El &#237;ndice de masa corporal se calcul&#243; por la divisi&#243;n del peso )kg) entre el cuadrado de la altura (m), consider&#225;ndose obesidad cuando &gt; 30. Medimos presi&#243;n arterial sist&#243;lica y diast&#243;lica, frecuencia card&#237;aca, peso y altura al momento del examen. El comit&#233; de &#233;tica en investigaci&#243;n de nuestra instituci&#243;n aprobaci&#243;n el protocolo del estudio y se obtuvo el consentimiento informado de todos los pacientes.</p>
      <p>
        <bold>Ecocardiograma Doppler</bold>
      </p>
      <p>Los ex&#225;menes se realizaron en d&#237;a interdial&#237;tico, con horario marcado entre 12 y 18 horas. Los pacientes se posicionaron en dec&#250;bito lateral izquierdo, utilizando ecocardi&#243;grafo Envisor C (Phillips Inc., Andover, Massachusetts, EEUU) equipado con transductores de 2-4 MHz para la realizaci&#243;n de estudio completo a los modos M, bidimensional y Doppler (puls&#225;til, continuo, coloreado y tisular). Los siguientes par&#225;metros se obtuvieron al modo M: di&#225;metro anteroposterior del atrio izquierdo, espesor del septo interventricular y de la pared posterior en la di&#225;stole, di&#225;metro diast&#243;lico final (dilataci&#243;n cuando &gt; 54 mm para mujeres y &gt; 56 mm para hombres) y sist&#243;lico final del VI. La masa ventricular izquierda fue estimada por la ecuaci&#243;n de Devereux<sup>9</sup> e indexada por la altura elevada &#224; 2,7<sup>10</sup>. Se defini&#243; como hipertrofia ventricular izquierda la presencia de masa/altura<sup>2,7</sup><underline>&gt;</underline> 45 g/m<sup>2,7</sup> para mujeres y <underline>&gt;</underline> 49 g/m<sup>2,7</sup> para hombres<sup>11</sup>. La funci&#243;n sist&#243;lica se evalu&#243; por el c&#225;lculo de la fracci&#243;n de eyecci&#243;n por el m&#233;todo de Simpson<sup>11</sup>. Las velocidad del flujo transvalvular mitral se registraron en el corte apical 4 c&#225;maras con la muestra del Doppler puls&#225;til posicionada entre las extremidades de las c&#250;spides de la v&#225;lvula mitral, midi&#233;ndose las velocidades de llenado r&#225;pido precoz (onda E), de contracci&#243;n atrial (onda A) y relaci&#243;n E/A. Las velocidades del Doppler tisular se registraron en el corte apical 4 c&#225;maras con una muestra del volumen posicionada consecutivamente en la uni&#243;n de las paredes lateral y septal del VI con el anillo mitral<sup>12</sup>. Se analizaron la velocidad diast&#243;lica precoz (E') y tard&#237;a (A') del anillo, y se calcularon las relaciones E'/A' y E/E' (promedio de los lados del anillo). El volumen del atrio izquierdo fue determinado al bidimensional por la t&#233;cnica biplanar de Simpson<sup>11</sup> e indexado para la superficie corp&#243;rea. En todas las medidas se consider&#243; el promedio de tres ciclos card&#237;acos.</p>
      <p>
        <bold>Evaluaci&#243;n de la funci&#243;n diast&#243;lica</bold>
      </p>
      <p>La funci&#243;n diast&#243;lica del VI fue categorizada a partir de la interpretaci&#243;n conjunta de los &#237;ndices derivados del Doppler convencional y Doppler tisular del anillo mitral en 4 patrones: normal, alteraci&#243;n de la relajaci&#243;n (relaci&#243;n E/A &lt; 1 y E&#180; &lt; 10 cm/s), seudonormal y flujo restrictivo (relaci&#243;n E/A &gt; 2 y E&#180; &lt; 8 cm/s)<sup>13</sup>. Para diagn&#243;stico del patr&#243;n seudonormal (diferenciando del normal veradero), se utilizaron los siguientes criterios: a) relaci&#243;n E/E' &gt; 15<sup>13</sup>; o b) relaci&#243;n E/E' <underline>&gt;</underline> 11<sup>12</sup>, asociada el &#237;ndice del volumen del atrio izquierdo &gt; 35 ml/m<sup>2,</sup>. La muestra se clasific&#243; posteriormente en tres grupos, de acuerdo con el patr&#243;n hemodin&#225;mico de llenado ventricular: 1) funci&#243;n diast&#243;lica normal, 2) DD discreta (DDD) (alteraci&#243;n de la relajaci&#243;n) y 3) DDA (englobando flujo restrictivo y seudonormalizaci&#243;n).</p>
      <p>
        <bold>An&#225;lisis de sobrevida</bold>
      </p>
      <p>Datos demogr&#225;ficos, comorbilidades (diabetes mellitus, hipertensi&#243;n arterial, dislipidemia, tabaquismo), drogas en uso y resultados de laboratorio rutinarios fueron levantados a partir de un riguroso an&#225;lisis de prontuario, adem&#225;s de entrevista con el m&#233;dico responsable, cuando era necesario. Los desenlaces primario y secundario fueron, respectivamente, mortalidad general y un combinado de eventos cardiovasculares fatales y no fatales. Los eventos investigados fueron muerte cardiovascular (incluyendo muerte s&#250;bita, infarto agudo de miocardio, Accidente vascular cerebral), infarto de miocardio no fatal e insuficiencia card&#237;aca congestiva descompensada (exigiendo internaci&#243;n hospitalaria). El seguimiento se bas&#243; en el an&#225;lisis de los desenlaces realizado de forma peri&#243;dica, directamente en la cl&#237;nica de di&#225;lisis. Pacientes que realizaron transplante renal o cambiaron la modalidad de di&#225;lisis fueron excluidos.</p>
      <p>
        <bold>An&#225;lisis estad&#237;stico</bold>
      </p>
      <p>Se aplic&#243; un an&#225;lisis descriptivo adecuado para variables continuas (promedio y desviaci&#243;n est&#225;ndar) y categ&#243;ricas (porcentaje). Se realizaron comparaciones entre los grupos por an&#225;lisis de varianza (ANOVA, con correcci&#243;n <italic>post hoc</italic> de Dunnett) para variables continuas, y por test chi-cuadrado para variables categ&#243;ricas. El an&#225;lisis de regresi&#243;n log&#237;stica determin&#243; los predictores independientes de la DD. Se construyeron curvas de sobrevida de Kaplan-Meier para el estado de la sobrevida y se compararon por el test <italic>log rank</italic>. El impacto pron&#243;stico independiente de la DD se evalu&#243; por el an&#225;lisis multivariado de sobrevida de Cox, tomando en cuenta predictores establecidos de riesgo en esta poblaci&#243;n. El nivel de significancia estad&#237;stica se defini&#243; como p &lt; 0,05. Se utilizaron los programas estad&#237;sticos <italic>SPSS 13 for Windows</italic> y <italic>JMP IN 5. 1</italic>.</p>
      <p>
        <bold>RESULTADOS</bold>
      </p>
      <p>
        <bold>Caracter&#237;sticas basales</bold>
      </p>
      <p>Las caracter&#237;sticas demogr&#225;ficas cl&#237;nicas, bioqu&#237;micas y de ecocardiograma Doppler de los 129 pacientes que formaron la poblaci&#243;n del estudio est&#225;n expuestas en la <xref ref-type="table" rid="t1-body3">Tabla 1</xref>. Nuestro grupo consisti&#243; en 78 hombres y 51 mujeres, con edad promedio de 52 &#177; 16 a&#241;os y duraci&#243;n de la di&#225;lisis de 7 &#177; 4 meses. La etiolog&#237;a de la ERC fue atribuida a nefroesclerosis hipertensiva (39%), nefropat&#237;a diab&#233;tica (21%), asociaci&#243;n de las dos anteriores (15%), glomerulonefritis cr&#243;nica (14%), ri&#241;&#243;n poliqu&#237;stico (5%), litiasis (3%), pielonefritis cr&#243;nica (2%) y otras afecciones (1%). La mayor&#237;a de los pacientes (77%) estaba en uso de medicaci&#243;n antihipertensiva, en especial inhibidores de la enzima conversora (46%), betabloqueadores (16%), alfabloqueadores (13%), antagonistas de los canales de calcio (12%) y bloqueadores de los receptores de la angiotensina (11%), aislados o en asociaci&#243;n.</p>
      <table-wrap id="t1-body3">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt01-es.jpg"/></table-wrap>
      <p>
        <bold>Alteraciones cl&#237;nicas y de ecocardiograma Doppler</bold>
      </p>
      <p>Al ingresar en el estudio, el 45% ten&#237;a hipertensi&#243;n arterial, el 34% diabetes mellitus, el 25% dislipidemia y el 11% eran fumadores. La prevalencia de obesidad (IMC &gt; 30) fue del 9%. La dilataci&#243;n del VI estaba presente en 34 pacientes (26%), hipertrofia en 110 (85%) y disfunci&#243;n sist&#243;lica en 24 (19%), aisladas o en asociaci&#243;n. S&#243;lo 19 (15%) presentaban geometr&#237;a normal del VI. En 58 individuos (45%) se encontr&#243; dilataci&#243;n significativa del atrio izquierdo (volumen &gt; 32ml/m<sup>2</sup>).</p>
      <p>
        <bold>Prevalencia de la disfunci&#243;n diast&#243;lica</bold>
      </p>
      <p>La DD fue diagnosticada en 94 de los 129 pacientes (73%), siendo 64 con DD discreta (50%) y 30 con DD avanzada (23%). En este &#250;ltimo grupo, hab&#237;a 20 pacientes con seudonormalizaci&#243;n y 10 con flujo restrictivo. En paralelo, s&#243;lo 22 (17%) presentaban relaci&#243;n E/E' promedio superior a 15. Al examinar exclusivamente las informaciones del Doppler convencional, s&#243;lo 80 de los 129 pacientes estudiados (62%) tendr&#237;an detectada la DD.</p>
      <p>
        <bold>Predictores de la DD avanzada</bold>
      </p>
      <p>Las principales diferencias entre los grupos con funci&#243;n diast&#243;lica normal, DD discreta y DD avanzada est&#225;n listadas en la <xref ref-type="table" rid="t2-body3">Tabla 2</xref>. Los individuos con DD avanzada ten&#237;an mayor edad (p &lt; 0,01), presi&#243;n arterial sist&#243;lica (p &lt; 0,01) y presi&#243;n arterial diast&#243;lica (0,043), masa del VI (p &lt; 0,01) e &#237;ndice del volumen del atrio izquierdo (p &lt; 0,01), as&#237; como mayor proporci&#243;n de diab&#233;ticos (p = 0,019) y menor promedio fracci&#243;n de eyecci&#243;n (p &lt; 0,01). Despu&#233;s del an&#225;lisis de regresi&#243;n log&#237;stica multivariado usando el grupo funci&#243;n normal como control, los predictores independientes de la DD avanzada fueron diabetes (odds ratio [OR] 2, IC 1,6-5,9, p = 0,011), presi&#243;n arterial sist&#243;lica (OR 1,05, IC 1,01-1,09, p = 0,023) y masa del VI (OR 1,06, intervalo de confianza [IC] 1,01-1,1, p &lt; 0,01), adem&#225;s de tendencia a fracci&#243;n de eyecci&#243;n (p = 0,052).</p>
      <table-wrap id="t2-body3">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt02-es.jpg"/></table-wrap>
      <p>
        <bold>Desenlaces</bold>
      </p>
      <p>Durante el seguimiento medio de 17 &#177; 7 meses, hubo 26 fallecimientos (20%) y 21 eventos cardiovasculares no fatales (16%). Las muertes fueron atribuidas a causas cardiovasculares (18 fallecimientos, siendo 8 por infarto de miocardio, 7 por muerte s&#250;bita, dos por arritmia ventricular compleja documentada y uno por accidente vascular cerebral hemorr&#225;gico) e infecciosas (8 fallecimientos). Los eventos cardiovasculares no fatales fueron infarto mioc&#225;rdico (5) e internaciones por insuficiencia card&#237;aca descompensada (16), contabilizando 39 eventos cardiovasculares combinados en total. Como se muestra en la <xref ref-type="fig" rid="f1-body3">Figura 1</xref> y en la <xref ref-type="table" rid="t3-body3">Tabla 3</xref>, la mortalidad general fue mayor en el grupo con DD avanzada (37%), en comparaci&#243;n a los normales y con DD discreta (9% y 19%, respectivamente, <italic>log rank test</italic>, p = 0,012). Varios an&#225;lisis fueron realizados utilizando modelos multivariados de Cox. Despu&#233;s de la evaluaci&#243;n de mortalidad general y eventos cardiovasculares en separado (modelos incluyendo edad, sexo masculino, diabetes, masa del VI y fracci&#243;n de eyecci&#243;n), masa y fracci&#243;n de eyecci&#243;n surgieron como predictores independientes para ambos desenlaces, adem&#225;s de la edad s&#243;lo para eventos cardiovasculares. La inclusi&#243;n de la DD avanzada en estos modelos alcanz&#243; valor estad&#237;stico significativo para la predicci&#243;n de eventos cardiovasculares (<italic>hazard ratio</italic> [HR] 2,2, IC 1,1-4,3, p = 0,021) y lim&#237;trofe para la mortalidad general (HR 2,8, IC 0,97-8,2, p = 0,056), como se vio en la <xref ref-type="table" rid="t4-body3">Tabla 4</xref>. En contraste, no hubo diferencias en los desenlaces entre pacientes con y sin relaci&#243;n E/E' &gt; 15 o E'&lt; 8 cm/s. En an&#225;lisis alternativo, DD avanzada e &#237;ndice del volumen de atrio izquierdo (recientemente descrito como predictor del pron&#243;stico en pacientes de HD<sup>15</sup>) fueron incluidos en conjunto en el &#250;ltimo paso del modelo. Fueron predictivos de eventos cardiovasculares tanto DD avanzada (HR 3,4, IC 1,3-9,2, p = 0,03) como &#237;ndice del volumen de atrio izquierdo (HR 6,6, IC 1,8-24, p = 0,004).</p>
      <fig id="f1-body3">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gf01-es.jpg"/></fig>
      <table-wrap id="t3-body3">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt03-es.jpg"/></table-wrap>
      <table-wrap id="t4-body3">
        <graphic xlink:href="1678-4170-abc-94-04-0457-00016-gt04-es.jpg"/></table-wrap>
      <p>
        <bold>Discusi&#243;n</bold>
      </p>
      <p>Nuestro estudio sugiere que casi tres cuartos de los individuos en el primero a&#241;o de HD tengan DD, siendo que en aproximadamente un cuarto de ellos existe DDA. Estudios con casu&#237;sticas reducidas reportaron prevalencia de DD en 50%-65% de los pacientes ur&#233;micos, incluyendo poblaciones predi&#225;lisis, en di&#225;lisis y post transplante<sup>4</sup> (porcentaje similar al encontrado en nuestro grupo, caso fueran consideradas las informaciones del Doppler tisular y volumen del atrio izquierdo). Tales an&#225;lisis fueron limitados por la utilizaci&#243;n de par&#225;metros derivados del flujo transvalvular mitral y del flujo venoso pulmonar para la categorizaci&#243;n de la funci&#243;n diast&#243;lica<sup>16</sup>. Se sabe que esos m&#233;todos son particularmente vulnerables a las variaciones de la precarga<sup>6</sup>, por lo tanto, tal abordaje puede haber inducido resultados falso negativos, diagnosticando como normales a portadores de seudonormalizaci&#243;n (altas presiones de llenado enmascarando la alteraci&#243;n de relajaci&#243;n del VI). En este contexto, integrar las informaciones del Doppler convencional con t&#233;cnicas relativamente independientes de la precarga, como el Doppler tisular y el volumen del atrio izquierdo, agrega precisi&#243;n al diagn&#243;stico de la DD, en especial de la DDA, caracterizada por alta presi&#243;n intraventricular diast&#243;lica. Detectar la presencia de la DD y estimar las presiones de llenado del VI es de inter&#233;s general en los d&#237;as actuales para la predicci&#243;n del riesgo de desarrollar la llamada "insuficiencia card&#237;aca con fracci&#243;n de eyecci&#243;n preservada". La insuficiencia card&#237;aca cl&#237;nicamente manifestada representa un predictor independiente de mortalidad en los pacientes iniciando terapia hemodial&#237;tica<sup>17</sup>, pero el discernimiento de la causa subyacente puede ser importante para orientar la conducta terap&#233;utica. Estudios de necropsia y uremia experimental se&#241;alaron la presencia de fibrosis intermioc&#225;rdica difusa espec&#237;fica en el coraz&#243;n de individuos ur&#233;micos, que podr&#237;a predisponer a la inestabilidad el&#233;ctrica (asociada con muerte s&#250;bita) y elevaci&#243;n de las presiones de llenado<sup>18,19</sup>. La intervenci&#243;n sobre los mecanismos fisiopatol&#243;gicos relacionados a la fibrosis mioc&#225;rdica prominente, como la activaci&#243;n de factores humorales (angiotensina II, hormona paratiroidea, endotelina, aldosterona y catecolaminas plasm&#225;ticas)<sup>3</sup>, podr&#225; representar un importante objetivo terap&#233;utico, en especial en la fase subcl&#237;nica.</p>
      <p>A pesar de tales consideraciones, poco se ha investigado sobre si el diagn&#243;stico de la DDA colabora para refinar la estratificaci&#243;n del riesgo cardiovascular en el paciente ur&#233;mico. Recientemente, dos estudios intentaron estimar el impacto pron&#243;stico de la DDA en la ERC utilizando la relaci&#243;n E/E', reconocido &#237;ndice no invasivo de las presiones de llenado del VI en la poblaci&#243;n general<sup>12,20</sup>. En un estudio con 125 candidatos al transplante renal, Sharma et al<sup>21</sup> encontraron una asociaci&#243;n de E/E' &gt; 15 con una mayor mortalidad general. Con todo, la poblaci&#243;n del estudio fue heterog&#233;nea (s&#243;lo un tercio de los pacientes estaba en HD) y s&#243;lo se realiz&#243; an&#225;lisis univariado, no permitiendo inferir si E/E' agrega valor pron&#243;stico a la evaluaci&#243;n tradicional de riesgo cardiovascular en este grupo. Ya Wang et al<sup>22</sup> relataron, en investigaci&#243;n con 220 pacientes (exclusivamente de di&#225;lisis peritoneal), que E/E' &gt; 15 fue capaz de prever mortalidad general y card&#237;aca en adici&#243;n a los datos cl&#237;nicos y ecocardiogr&#225;ficos cl&#225;sicos. En nuestra poblaci&#243;n, compuesta s&#243;lo por pacientes en HD, la relaci&#243;n E/E' &gt; 15 no tuvo poder discriminador con relaci&#243;n a los desenlaces estudiados. La fisiopatolog&#237;a de la enfermedad cardiovascular en individuos en HD se ve influenciada por las abruptas y extensas variaciones de la volemia a las cuales son sometidos estos pacientes<sup>23</sup>. La predicci&#243;n exacta de las presiones de llenado (y, por consiguiente, del pron&#243;stico) para un individuo dado exige la incorporaci&#243;n de todos los datos disponibles, lo que hace el abordaje integrado m&#225;s consistente que un par&#225;metro tomado aisladamente.</p>
      <p>Entre las limitaciones del estudio, es importante mencionar el tama&#241;o relativamente limitado de la muestra, que fue contrabalanceado, sin embargo, por el adecuado poder estad&#237;stico alcanzado (86% para desenlace primario y 94% para secundario). Otras limitaciones fueron la ausencia de medidas invasivas de las presiones de llenado del VI (aspectos pr&#225;cticos y &#233;ticos no justificar&#237;an cateterismo card&#237;aco en la poblaci&#243;n estudiada) y el rigor de los criterios de exclusi&#243;n (que pueden haber transformado nuestros hallazgos en no aplicables a la totalidad de la poblaci&#243;n en di&#225;lisis).</p>
      <p>
        <bold>Conclusiones</bold>
      </p>
      <p>El presente estudio indica que la DDA, diagnosticada a partir de la interpretaci&#243;n combinada de las informaciones de ecocardiograma Doppler, conlleva impacto pron&#243;stico en pacientes en HD sin eventos cardiovasculares previos. La mortalidad general fue significativamente mayor en el grupo con DDA, en comparaci&#243;n con los normales y con DD discreta. Paralelamente, la DDA fue predictiva de eventos cardiovasculares independientemente de edad, sexo, diabetes, masa del VI y fracci&#243;n de eyecci&#243;n.</p>
      <p>
        <bold>Potencial Conflicto de Intereses</bold>
      </p>
      <p>Declaro no haber conflicto de intereses pertinentes.</p>
      <p>
        <bold>Fuentes de Financiaci&#243;n</bold>
      </p>
      <p>El presente estudio fue parcialmente financiado por Beca de apoyo para investigaci&#243;n en cardiolog&#237;a de la SBC.</p>
      <p>
        <bold>Vinculaci&#243;n Acad&#233;mica</bold>
      </p>
      <p>No hay vinculaci&#243;n de este estudio a programas de postgrado.</p>
      <p>
        <bold>Referencias</bold>
      </p>
    </body>
  </sub-article>
</article>
